A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035021



Internal ID18777552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80559891..80596256hg38UCSC Ensembl
Innerchr5:79855710..79892075hg19UCSC Ensembl
Innerchr5:79891466..79927831hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3836366
hg1936366
hg1836366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5706n100
Supporting Variantsnssv3639132
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)nsv1035021
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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