A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023695



Internal ID16317651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5140234..5140857hg38UCSC Ensembl
Innerchr5:5140347..5140970hg19UCSC Ensembl
Innerchr5:5193347..5193970hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596940
Supporting Variants
Samples
Known GenesADAMTS16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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