A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623064



Internal ID7009921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44535964..44537968hg38UCSC Ensembl
Innerchr10:44535964..44537968hg38UCSC Ensembl
Outerchr10:44535697..44538223hg38UCSC Ensembl
chr10:45031412..45033416hg19UCSC Ensembl
Innerchr10:45031412..45033416hg19UCSC Ensembl
Outerchr10:45031145..45033671hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13765010, essv13765009, essv13765008, essv13765005, essv13765007, essv13765006
SamplesHG00542, HG02409, HG01810, HG00584, HG01804, HG00595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623064
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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