A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694532



Internal ID15431184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44898921..44909942hg38UCSC Ensembl
Innerchr3:44940413..44951434hg19UCSC Ensembl
Innerchr3:44915417..44926438hg18UCSC Ensembl
Innerchr3:44915417..44926438hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3811022
hg1911022
hg1811022
hg1711022
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521765
Supporting Variants
Samples
Known GenesTGM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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