A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060889



Internal ID18803420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27765442hg38UCSC Ensembl
Innerchr19:27747981..28256350hg19UCSC Ensembl
Innerchr19:32439821..32948190hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38508370
hg19508370
hg18508370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n100
Supporting Variantsnssv3572039
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)nsv1060889
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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