A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019666



Internal ID19108884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:77480544..77598122hg38UCSC Ensembl
Innerchr5:76776369..76893947hg19UCSC Ensembl
Innerchr5:76812125..76929703hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38117579
hg19117579
hg18117579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5704n100
Supporting Variantsnssv3639045
Samples
Known GenesWDR41
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019666
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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