A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574995



Internal ID16362404
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 StatusM
Merged Variants
Supporting Variantsnssv870536
Samples
Known GenesKRT25, KRT26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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