A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032733



Internal ID19121955
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 StatusM
Merged Variants
Supporting Variantsnssv3649125
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)nsv1032733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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