A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875740



Internal ID15823010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61137221..61227472hg38UCSC Ensembl
Innerchr17:59214582..59304833hg19UCSC Ensembl
Innerchr17:56569364..56659615hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3890252
hg1990252
hg1890252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575839
Supporting Variants
Samples
Known GenesBCAS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875740
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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