A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870536



Internal ID16164492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40722575..40767383hg38UCSC Ensembl
Innerchr17:38878827..38923635hg19UCSC Ensembl
Innerchr17:36132353..36177161hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3844809
hg1944809
hg1844809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574995
Supporting Variants
Samples
Known GenesKRT25, KRT26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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