A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575873



Internal ID16363282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65327463..65375762hg38UCSC Ensembl
Innerchr17:63323581..63371880hg19UCSC Ensembl
Innerchr17:60754043..60802342hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3848300
hg1948300
hg1848300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875821
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575873
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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