A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622837



Internal ID6663006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32703158..32706680hg38UCSC Ensembl
Innerchr10:32703158..32706680hg38UCSC Ensembl
Outerchr10:32702862..32706950hg38UCSC Ensembl
chr10:32992086..32995608hg19UCSC Ensembl
Innerchr10:32992086..32995608hg19UCSC Ensembl
Outerchr10:32991790..32995878hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383523
hg193523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13750483, essv13750486, essv13750487, essv13750485, essv13750488, essv13750484, essv13750482
SamplesHG00346, HG00123, HG00281, HG00285, NA12842, HG00376, HG00327
Known GenesCCDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622837
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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