A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688972



Internal ID15425624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161700078..161829856hg38UCSC Ensembl
Innerchr3:161417866..161547644hg19UCSC Ensembl
Innerchr3:162900560..163030338hg18UCSC Ensembl
Innerchr3:162900568..163030346hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38129779
hg19129779
hg18129779
hg17129779
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515615
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688972
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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