A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633199



Internal ID18584794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17630..137401hg38UCSC Ensembl
Innerchr5:17630..137516hg19UCSC Ensembl
Innerchr5:70630..190516hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38119772
hg19119887
hg18119887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026232
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)nssv3633199
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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