A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697279



Internal ID15433931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172555654..172555722hg38UCSC Ensembl
Innerchr3:172273444..172273512hg19UCSC Ensembl
Innerchr3:173756138..173756206hg18UCSC Ensembl
Innerchr3:173756146..173756214hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
hg1769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520203
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697279
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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