A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622921



Internal ID7009779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36360120..36361776hg38UCSC Ensembl
Innerchr10:36360155..36361742hg38UCSC Ensembl
Outerchr10:36360086..36361811hg38UCSC Ensembl
chr10:36649048..36650704hg19UCSC Ensembl
Innerchr10:36649083..36650670hg19UCSC Ensembl
Outerchr10:36649014..36650739hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381657
hg191657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756427
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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