A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913047



Internal ID4722587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101258722..101264885hg38UCSC Ensembl
Innerchr10:101259222..101264385hg38UCSC Ensembl
Outerchr10:101257722..101265885hg38UCSC Ensembl
chr10:103018479..103024642hg19UCSC Ensembl
Innerchr10:103018979..103024142hg19UCSC Ensembl
Outerchr10:103017479..103025642hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386164
hg196164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624373
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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