A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149792



Internal ID15877402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68791287..68821725hg38UCSC Ensembl
Innerchr17:66787428..66817866hg19UCSC Ensembl
Innerchr17:64299023..64329461hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3830439
hg1930439
hg1830439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575927
Supporting Variants
SamplesHGDP00983
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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