A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015884



Internal ID18758418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172653521..172753954hg38UCSC Ensembl
Innerchr5:172080524..172180957hg19UCSC Ensembl
Innerchr5:172013129..172113562hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38100434
hg19100434
hg18100434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5831n100
Supporting Variantsnssv3649138
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015884
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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