A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021474



Internal ID16315430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1008649..1009348hg38UCSC Ensembl
Innerchr5:1008764..1009463hg19UCSC Ensembl
Innerchr5:1061764..1062463hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596794
Supporting Variants
Samples
Known GenesNKD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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