A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622841



Internal ID6663010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32852471..32853047hg38UCSC Ensembl
Innerchr10:32852485..32853033hg38UCSC Ensembl
Outerchr10:32852457..32853061hg38UCSC Ensembl
chr10:33141399..33141975hg19UCSC Ensembl
Innerchr10:33141413..33141961hg19UCSC Ensembl
Outerchr10:33141385..33141989hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13751192, essv13751191, essv13751193
SamplesHG03378, HG03442, HG03583
Known GenesCCDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622841
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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