A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647219



Internal ID18945500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117668542..117726050hg38UCSC Ensembl
Innerchr5:117004237..117061745hg19UCSC Ensembl
Innerchr5:117032136..117089644hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3857509
hg1957509
hg1857509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027932
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)nssv3647219
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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