A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv923e199



Internal ID20124225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9156428..9230320hg38UCSC Ensembl
chr4:9158154..9232046hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3873893
hg1973893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678265, esv2668726
SamplesHG01357, HG00613, HG01441, NA19012, NA12718, HG00313, HG00152, HG00734, HG01359, NA19436, HG00318, NA18616, HG00182, NA19904, HG00344, NA18530, NA18630, NA19081, NA19819, HG00328, HG01055, HG00705, NA07056, NA18874, HG00437, HG01342, HG01173, HG00171, HG00369, HG01083, HG00112, HG00731, HG00186, NA12347, NA19783, NA20508, HG00160, NA19060, NA19469, HG00310, NA19003, NA06989, HG01079, NA12340, HG01389, HG00463, HG01197, HG00657, HG01365, NA19453, NA19451, NA20816, HG01488, NA19010, HG00173, HG00148, NA19920, NA20778, HG01350, HG00190, HG00106, HG00698, HG01188, HG00581, HG01204, NA18963, HG00187, HG01461, NA19648, NA19004, HG00280, HG00335, HG01134, HG00366, HG00578, HG00331, NA19701, HG00737, NA19084, NA12341, HG00156, NA18950, HG00188, NA18626, NA19776, NA20586, HG00247, HG00554, HG01133, HG00592, HG00244, NA19077, HG01107, NA19062, NA19726, HG01148, NA19067, NA19982, NA19085, HG00179, HG01140, NA19059, NA20819, HG00593, NA11994, NA19660, HG00638, NA18622, HG00180, NA19471, NA19900, HG01048, NA19444, NA19722, NA18617, HG00372, HG00692, NA20754, HG01124, NA19083, HG00141, NA12273, NA07048, NA19440, NA19908, NA19066, HG00150, HG00258, NA11843, HG01136, NA12400, NA19835, HG00243, NA19679, HG00403, HG01187, NA19457, NA18634, NA19700, NA20589, HG00343, NA19082, HG00584, NA19684, HG00133, HG00662, NA19000, NA19055, NA19676, HG00373, NA19725, HG00620, NA19313, HG01437, NA19080, HG00108, NA18620, HG01465, NA19372, HG00653, NA19703, HG00640, HG00732, NA12348, HG00185, HG00559, NA12275, NA19657, HG01073, NA18977, HG00239, NA19664, HG00265, NA19901, HG01170, NA19704, NA20818, NA18487, NA18961, NA20828, HG01080, NA20815, HG00740, NA18988, NA18562, HG01060, HG01383, NA18985, HG01149, HG00120, HG00151, NA18619, NA18987, NA18999, HG01137, NA19921, HG00595, NA20534, NA19723, NA19078, HG00650, NA18565, NA19009, HG00663, HG00262, NA18631, NA18989, HG00580, NA19719, NA19434, HG01390, NA19452, HG00123, NA19063, NA12546, NA19655, HG00142, NA19371, NA19070, HG00367, NA18984, HG00693, HG00566, HG01125, NA19130, HG00119, HG00320, HG00275, HG00324, HG00625, HG00690, HG00641, NA18574, HG00183, HG00473, NA19350, HG01462, NA18908, NA19473, HG01377, NA18615, HG00336, HG00272, NA19468, HG00704, NA19007, NA19661, NA19058, NA19466, HG01067, HG01354, NA19439, HG00312, HG00327, HG00361, HG01198
Known GenesUSP17L10, USP17L11, USP17L12, USP17L13, USP17L18, USP17L20, USP17L21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv923e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss256
Observed Complex0
Frequencyn/a


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