A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575829



Internal ID16016552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60812316..60945034hg38UCSC Ensembl
Innerchr17:58889677..59022395hg19UCSC Ensembl
Innerchr17:56244459..56377177hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38132719
hg19132719
hg18132719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875715, nssv875716
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575829
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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