A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063389



Internal ID19152608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41519342..41579831hg38UCSC Ensembl
Innerchr17:39675594..39736083hg19UCSC Ensembl
Innerchr17:36929120..36989609hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3860490
hg1960490
hg1860490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719439
Samples
Known GenesKRT19, KRT9, LINC00974
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063389
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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