A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149769



Internal ID15854714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51417214..51477734hg38UCSC Ensembl
Innerchr17:49494575..49555095hg19UCSC Ensembl
Innerchr17:46849574..46910094hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3860521
hg1960521
hg1860521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575527
Supporting Variants
Samples1780862301_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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