A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639649



Internal ID18937930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8271189..8291192hg38UCSC Ensembl
Innerchr5:8271302..8291305hg19UCSC Ensembl
Innerchr5:8324302..8344305hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3820004
hg1920004
hg1820004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023430
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)nssv3639649
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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