A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868972



Internal ID16162928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26936341..26955229hg38UCSC Ensembl
Innerchr17:25263367..25282255hg19UCSC Ensembl
Innerchr17:22287494..22306382hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3818889
hg1918889
hg1818889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574632
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)nssv868972
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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