A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv923e199

Internal ID20124225
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9156428..9230320hg38UCSC Ensembl
chr4:9158154..9232046hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv923e199
Sample Size1151
Observed Gain0
Observed Loss256
Observed Complex0

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