A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026302



Internal ID16320258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17347597..17353890hg38UCSC Ensembl
Innerchr5:17347706..17353999hg19UCSC Ensembl
Innerchr5:17400706..17406999hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386294
hg196294
hg186294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597316
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)nssv1026302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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