A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026232



Internal ID18768764
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 StatusM
Merged Variantsdgv5514n100
Supporting Variantsnssv3633199
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)nsv1026232
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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