A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649125



Internal ID18947406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170164317..170189362hg38UCSC Ensembl
Innerchr5:169591321..169616366hg19UCSC Ensembl
Innerchr5:169523899..169548944hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3825046
hg1925046
hg1825046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032733
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649125
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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