A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022266



Internal ID19111484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99326944..99732957hg38UCSC Ensembl
Innerchr5:98662648..99068661hg19UCSC Ensembl
Innerchr5:98690547..99096560hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38406014
hg19406014
hg18406014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640478
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022266
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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