A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1334e199



Internal ID22759107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32711065..32731785hg38UCSC Ensembl
chr9:32711063..32731783hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820721
hg1920721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2671053, esv2669974, esv2657920
SamplesHG00626, NA19701, HG00650, HG01173, HG00231, NA19397, NA19664, HG01359, NA12273, HG00187, HG01188, NA19734, HG01066, HG00233, NA18528, NA19359, HG01465, HG00699, NA20294, NA20332, HG00179, NA18616, HG00150, HG01140, HG00693, HG00641, NA19076, HG01366, HG01070, HG00272, HG00689, HG00458, HG01492, HG01354, NA19088, HG01083, HG00247, NA19782, HG00185, NA19079, HG01134, HG01455, NA20518, NA20278, HG00335, NA20819, NA18977, NA19371, HG00705, NA19087, HG00182, NA19002, HG01198, HG00637, HG01048, HG01133, HG00178, HG00739, HG00464, HG01124, HG00313, HG01136, HG00149, NA20800, HG00183, HG00176, HG01187, HG00282, NA19077, HG01515, HG00320, HG00584, HG00533, HG01345, HG00692, HG00635, HG01390, HG01047, HG00324, HG00284, HG01073, NA20299, NA18626, HG00404, HG01383, HG01101, NA18553, HG01334, HG00704, HG00463, NA19469, NA18634, NA20296, NA19685, HG00285, HG00265, NA19749, HG00565, NA18628, NA19732, NA12272, HG01253, HG00734, NA19435, NA18941, NA19010, HG00098, HG01137, HG00116, HG01108, NA20281, HG00662, HG00418, NA19085, HG00620, HG00614, HG00578, HG01491, NA18631, NA19438, NA19223, NA19474, HG00174, NA20786, HG00112, HG00698, HG01251, HG00372, HG01378, HG01111, HG00171, NA19063, HG01191, HG00180
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1334e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss134
Observed Complex0
Frequencyn/a


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