A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870553



Internal ID16164509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41041489..41064785hg38UCSC Ensembl
Innerchr17:39197741..39221037hg19UCSC Ensembl
Innerchr17:36451267..36474563hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3823297
hg1923297
hg1823297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575007
Supporting Variants
Samples
Known GenesKRTAP2-1, KRTAP2-2, KRTAP2-3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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