A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863967



Internal ID3865783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75387876..75389872hg38UCSC Ensembl
Innerchr10:75387919..75389829hg38UCSC Ensembl
Outerchr10:75387833..75389915hg38UCSC Ensembl
chr10:77147634..77149630hg19UCSC Ensembl
Innerchr10:77147677..77149587hg19UCSC Ensembl
Outerchr10:77147591..77149673hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381997
hg191997
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623849
Supporting Variants
SamplesHG02573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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