A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622956



Internal ID7009814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37440034..37598028hg38UCSC Ensembl
chr10:37728962..37886956hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38157995
hg19157995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756803
SamplesHG00473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622956
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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