A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696010



Internal ID15432662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170182185..170199025hg38UCSC Ensembl
Innerchr4:171103336..171120176hg19UCSC Ensembl
Innerchr4:171339911..171356751hg18UCSC Ensembl
Innerchr4:171478066..171494906hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3816841
hg1916841
hg1816841
hg1716841
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518567
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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