A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574925



Internal ID16362334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36885885..36893045hg38UCSC Ensembl
Innerchr17:35243142..35250306hg19UCSC Ensembl
Innerchr17:32317255..32324419hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387161
hg197165
hg187165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870165
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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