A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062354



Internal ID19151573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41510342..41540800hg38UCSC Ensembl
Innerchr17:39666594..39697052hg19UCSC Ensembl
Innerchr17:36920120..36950578hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3830459
hg1930459
hg1830459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545109
Samples
Known GenesKRT15, KRT19, MIR6510
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062354
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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