A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021228



Internal ID16315184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:468129..472407hg38UCSC Ensembl
Innerchr5:468244..472522hg19UCSC Ensembl
Innerchr5:521244..525522hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384279
hg194279
hg184279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596670
Supporting Variants
Samples
Known GenesPP7080
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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