A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663321



Internal ID15399973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62663603..62689654hg38UCSC Ensembl
Innerchr17:60740964..60767015hg19UCSC Ensembl
Innerchr17:58094696..58120747hg18UCSC Ensembl
Innerchr17:58094696..58120747hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3826052
hg1926052
hg1826052
hg1726052
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516921
Supporting Variants
Samples
Known GenesMRC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663321
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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