A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021499



Internal ID18764033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160531332..160735337hg38UCSC Ensembl
Innerchr5:159958339..160162344hg19UCSC Ensembl
Innerchr5:159890917..160094922hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38204006
hg19204006
hg18204006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648228
Samples
Known GenesATP10B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021499
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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