A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017366



Internal ID19106583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56361382..56376272hg38UCSC Ensembl
Innerchr5:55657209..55672099hg19UCSC Ensembl
Innerchr5:55692966..55707856hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3814891
hg1914891
hg1814891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642145
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)nsv1017366
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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