A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021594



Internal ID16315550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1178396..1180053hg38UCSC Ensembl
Innerchr5:1178511..1180168hg19UCSC Ensembl
Innerchr5:1231511..1233168hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381658
hg191658
hg181658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596836
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)nssv1021594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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