A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034832



Internal ID18777365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80548436..80596256hg38UCSC Ensembl
Innerchr5:79844255..79892075hg19UCSC Ensembl
Innerchr5:79880011..79927831hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3847821
hg1947821
hg1847821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5706n100
Supporting Variantsnssv3639072
Samples
Known GenesANKRD34B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034832
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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