A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868978



Internal ID16162934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26938439..26955229hg38UCSC Ensembl
Innerchr17:25265465..25282255hg19UCSC Ensembl
Innerchr17:22289592..22306382hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3816791
hg1916791
hg1816791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574637
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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