A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695641



Internal ID15432293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14490517..14502161hg38UCSC Ensembl
Innerchr3:14532025..14543669hg19UCSC Ensembl
Innerchr3:14507029..14518673hg18UCSC Ensembl
Innerchr3:14507029..14518673hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3811645
hg1911645
hg1811645
hg1711645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518216
Supporting Variants
Samples
Known GenesGRIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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