A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574625



Internal ID16362034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22743389..22763458hg38UCSC Ensembl
Innerchr17:22242716..22262785hg19UCSC Ensembl
Innerchr17:22166843..22186912hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3820070
hg1920070
hg1820070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868963
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574625
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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