A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149800



Internal ID15872704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71364730..71391319hg38UCSC Ensembl
Innerchr17:69360871..69387460hg19UCSC Ensembl
Innerchr17:66872466..66899055hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3826590
hg1926590
hg1826590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575953
Supporting Variants
SamplesHGDP00019
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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