A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13867011



Internal ID939206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78915579..78921261hg38UCSC Ensembl
Innerchr10:78915579..78921261hg38UCSC Ensembl
Outerchr10:78915297..78921409hg38UCSC Ensembl
chr10:80675336..80681018hg19UCSC Ensembl
Innerchr10:80675336..80681018hg19UCSC Ensembl
Outerchr10:80675054..80681166hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385683
hg195683
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623904
Supporting Variants
SamplesHG00560
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13867011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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