A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697247



Internal ID15433899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:137224272..137228884hg38UCSC Ensembl
Innerchr8:138236515..138241127hg19UCSC Ensembl
Innerchr8:138305697..138310309hg18UCSC Ensembl
Innerchr8:138305697..138310309hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg384613
hg194613
hg184613
hg174613
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697247
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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