A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023678



Internal ID16317634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3591128..3595628hg38UCSC Ensembl
Innerchr5:3591242..3595742hg19UCSC Ensembl
Innerchr5:3644242..3648742hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384501
hg194501
hg184501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596921
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)nssv1023678
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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