A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662190



Internal ID9928295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62602315..62605921hg38UCSC Ensembl
Outerchr9:62601944..62606291hg38UCSC Ensembl
Innerchr9:46913616..46917222hg19UCSC Ensembl
Outerchr9:46913245..46917592hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1349e199
Supporting Variantsessv5667466, essv6583294, essv6359020, essv5973110, essv5712211, essv6354505, essv6138223, essv6141536, essv6459026, essv5831657, essv6518291, essv5696137, essv6000982, essv5585326, essv6160498, essv5969372, essv6020037, essv6300965, essv5478582, essv6525503, essv5452530, essv5562472, essv5967559, essv5407489, essv6171224, essv5428170, essv5738964, essv6181740, essv5666994, essv6185906, essv6019028, essv6531512, essv6160445, essv5671734, essv5696751, essv5411296, essv6007517, essv6325083, essv5609165, essv5702536, essv5503491, essv6584559, essv5564973, essv5672395, essv5605762, essv6281941, essv5741530, essv6467893, essv6118204, essv6379961, essv6159848, essv5420589, essv6206554, essv6543579, essv5542672
SamplesHG00593, HG00626, HG00403, HG00650, HG00542, HG00536, HG00608, HG00449, HG00663, HG00589, HG00501, HG00702, HG00689, HG00610, HG00512, HG00422, HG00705, HG00530, HG00419, HG00543, HG00560, HG00629, HG00443, HG00557, HG00428, HG00653, HG00701, HG00475, HG00556, HG00583, HG00619, HG00692, HG00651, HG00404, HG00531, HG00479, HG00684, HG00525, HG00704, HG00463, HG00611, HG00476, HG00565, HG00473, HG00607, HG00662, HG00418, HG00707, HG00614, HG00513, HG00478, HG00421, HG00656, HG00472, HG00628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662190
Frequency
Sample Size1151
Observed Gain0
Observed Loss55
Observed Complex0
Frequencyn/a


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