A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694474



Internal ID15431126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6374338..6374568hg38UCSC Ensembl
Innerchr17:6277658..6277888hg19UCSC Ensembl
Innerchr17:6218382..6218612hg18UCSC Ensembl
Innerchr17:6218382..6218612hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38231
hg19231
hg18231
hg17231
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521701
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694474
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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