A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149729



Internal ID15875465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14363680..14389591hg38UCSC Ensembl
Innerchr17:14266997..14292908hg19UCSC Ensembl
Innerchr17:14207722..14233633hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3825912
hg1925912
hg1825912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574424
Supporting Variants
SamplesHGDP00686
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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