A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575008



Internal ID16362417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41041489..41065044hg38UCSC Ensembl
Innerchr17:39197741..39221296hg19UCSC Ensembl
Innerchr17:36451267..36474822hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3823556
hg1923556
hg1823556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5591n54
Supporting Variantsnssv870555, nssv870556, nssv870554
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)nsv575008
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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