A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13756669



Internal ID3415358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36563329..36573009hg38UCSC Ensembl
Innerchr10:36563355..36572984hg38UCSC Ensembl
Outerchr10:36563304..36573035hg38UCSC Ensembl
chr10:36852257..36861937hg19UCSC Ensembl
Innerchr10:36852283..36861912hg19UCSC Ensembl
Outerchr10:36852232..36861963hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg389681
hg199681
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622928
Supporting Variants
SamplesHG03057
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13756669
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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