A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574894



Internal ID16362303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36346709..36356337hg38UCSC Ensembl
Innerchr17:34651852..34661472hg19UCSC Ensembl
Innerchr17:31675965..31685585hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389629
hg199621
hg189621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870134, nssv870133
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574894
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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