A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575001



Internal ID16362410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40977888..40982248hg38UCSC Ensembl
Innerchr17:39134140..39138500hg19UCSC Ensembl
Innerchr17:36387666..36392026hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg384361
hg194361
hg184361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870542
Samples
Known GenesKRT40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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