A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026335



Internal ID16320291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17351166..17353890hg38UCSC Ensembl
Innerchr5:17351275..17353999hg19UCSC Ensembl
Innerchr5:17404275..17406999hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382725
hg192725
hg182725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597322
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1026335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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