A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574996



Internal ID16362405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40727480..40752940hg38UCSC Ensembl
Innerchr17:38883732..38909192hg19UCSC Ensembl
Innerchr17:36137258..36162718hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3825461
hg1925461
hg1825461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870537
Samples
Known GenesKRT25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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