A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622584



Internal ID7009442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21494192..21501191hg38UCSC Ensembl
Innerchr10:21494192..21501191hg38UCSC Ensembl
Outerchr10:21493692..21501691hg38UCSC Ensembl
chr10:21783121..21790120hg19UCSC Ensembl
Innerchr10:21783121..21790120hg19UCSC Ensembl
Outerchr10:21782621..21790620hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13715460, essv13715464, essv13715459, essv13715465, essv13715458, essv13715456, essv13715457, essv13715461, essv13715463, essv13715462
SamplesHG02496, HG00306, NA19443, NA18995, HG01277, NA19036, NA20412, NA18747, NA18992, NA19117
Known GenesCASC10, MIR1915
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622584
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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