A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574692



Internal ID16015415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32153328..32281827hg38UCSC Ensembl
Innerchr17:30480347..30608846hg19UCSC Ensembl
Innerchr17:27504460..27632959hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38128500
hg19128500
hg18128500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869602
Samples
Known GenesRHBDL3, RHOT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574692
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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