A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575751



Internal ID16363160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57132067..57143588hg38UCSC Ensembl
Innerchr17:55209428..55220949hg19UCSC Ensembl
Innerchr17:52564427..52575948hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811522
hg1911522
hg1811522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874641
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575751
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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