A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568603



Internal ID18866884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48657855..48697278hg38UCSC Ensembl
Innerchr17:46735217..46774640hg19UCSC Ensembl
Innerchr17:44090216..44129639hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3839424
hg1939424
hg1839424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060931
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568603
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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