A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875741



Internal ID16169697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61735387..61837320hg38UCSC Ensembl
Innerchr17:59812748..59914681hg19UCSC Ensembl
Innerchr17:57167530..57269463hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38101934
hg19101934
hg18101934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575841
Supporting Variants
Samples
Known GenesBRIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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