A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682376



Internal ID15072342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4106646..4140066hg38UCSC Ensembl
Innerchr3:4148330..4181750hg19UCSC Ensembl
Innerchr3:4123330..4156750hg18UCSC Ensembl
Innerchr3:4123330..4156750hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3833421
hg1933421
hg1833421
hg1733421
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682376
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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