A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702826



Internal ID15439478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86573367..86776719hg38UCSC Ensembl
Innerchr14:87039711..87243063hg19UCSC Ensembl
Innerchr14:86109464..86312816hg18UCSC Ensembl
Innerchr14:86109464..86312816hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38203353
hg19203353
hg18203353
hg17203353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526516
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702826
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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