A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623515



Internal ID7010371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63873737..63874602hg38UCSC Ensembl
Innerchr10:63873738..63874602hg38UCSC Ensembl
Outerchr10:63873737..63874603hg38UCSC Ensembl
chr10:65633497..65634362hg19UCSC Ensembl
Innerchr10:65633498..65634362hg19UCSC Ensembl
Outerchr10:65633497..65634363hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13836135, essv13836167, essv13836158, essv13836132, essv13836126, essv13836176, essv13836136, essv13836174, essv13836134, essv13836120, essv13836154, essv13836130, essv13836185, essv13836115, essv13836138, essv13836128, essv13836147, essv13836162, essv13836116, essv13836157, essv13836169, essv13836171, essv13836161, essv13836188, essv13836189, essv13836140, essv13836114, essv13836168, essv13836150, essv13836159, essv13836182, essv13836124, essv13836121, essv13836181, essv13836183, essv13836177, essv13836153, essv13836184, essv13836119, essv13836175, essv13836186, essv13836122, essv13836179, essv13836123, essv13836118, essv13836129, essv13836146, essv13836155, essv13836113, essv13836133, essv13836170, essv13836187, essv13836166, essv13836145, essv13836160, essv13836131, essv13836139, essv13836165, essv13836178, essv13836152, essv13836144, essv13836141, essv13836127, essv13836142, essv13836172, essv13836149, essv13836125, essv13836164, essv13836137, essv13836180, essv13836148, essv13836117, essv13836156, essv13836151, essv13836173, essv13836143, essv13836163
SamplesNA18998, HG00881, HG00189, HG01850, HG00442, HG02072, HG00231, HG00524, HG02035, HG02029, HG02061, NA18596, NA18625, NA18616, NA18962, NA18988, NA18563, HG02016, HG02140, NA18619, HG00458, HG00330, HG01599, HG00634, HG02130, HG00851, NA18642, NA18582, NA18571, HG00277, HG00632, NA19087, HG02190, HG02178, NA19002, HG02138, NA18954, NA18638, NA18648, NA18614, NA18747, HG00443, HG00268, HG00266, HG00176, HG00282, HG00596, HG02142, HG02057, HG01810, NA19081, NA18637, HG01796, NA19064, NA18757, HG01311, HG00844, HG00531, HG00479, NA18946, NA18963, HG00704, HG00410, HG00445, HG00407, HG00476, NA18564, NA19380, HG00620, HG02128, NA18971, NA18631, NA18987, HG02182, HG00628, HG00171, HG00759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623515
Frequency
Sample Size2504
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


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