A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574699



Internal ID16362108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32486209..32486852hg38UCSC Ensembl
Innerchr17:30813227..30813870hg19UCSC Ensembl
Innerchr17:27837340..27837983hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38644
hg19644
hg18644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869610, nssv869609
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574699
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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