A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022198



Internal ID15969468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1552140..1624236hg38UCSC Ensembl
Innerchr5:1552255..1624351hg19UCSC Ensembl
Innerchr5:1605255..1677351hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3872097
hg1972097
hg1872097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596885
Supporting Variants
Samples
Known GenesLOC728613, SDHAP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1022198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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