A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019519



Internal ID18762054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180439730..180532408hg38UCSC Ensembl
Innerchr5:179866730..179959408hg19UCSC Ensembl
Innerchr5:179799336..179892014hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3892679
hg1992679
hg1892679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649318
Samples
Known GenesCNOT6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019519
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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