A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020985



Internal ID18763519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:71184..138345hg38UCSC Ensembl
Innerchr5:71299..138460hg19UCSC Ensembl
Innerchr5:124299..191460hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3867162
hg1967162
hg1867162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5519n100
Supporting Variantsnssv3633210
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)nsv1020985
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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