A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654641



Internal ID15044607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36459737..36526355hg38UCSC Ensembl
Innerchr17:34815551..34882186hg19UCSC Ensembl
Innerchr17:31889664..31956299hg18UCSC Ensembl
Innerchr17:31889664..31956299hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3866619
hg1966636
hg1866636
hg1766636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516100
Supporting Variants
Samples
Known GenesMYO19, ZNHIT3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654641
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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