A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575037



Internal ID16362446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41376845..41382941hg38UCSC Ensembl
Innerchr17:39533097..39539193hg19UCSC Ensembl
Innerchr17:36786623..36792719hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg386097
hg196097
hg186097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv871840
Samples
Known GenesKRT34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575037
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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