A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868971



Internal ID16162927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26936341..26941061hg38UCSC Ensembl
Innerchr17:25263367..25268087hg19UCSC Ensembl
Innerchr17:22287494..22292214hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg384721
hg194721
hg184721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574631
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)nssv868971
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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