A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675734



Internal ID15412386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75333283..75379524hg38UCSC Ensembl
Innerchr3:75382434..75428675hg19UCSC Ensembl
Innerchr3:75465124..75511365hg18UCSC Ensembl
Innerchr3:75465124..75511365hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3846242
hg1946242
hg1846242
hg1746242
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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