A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057162



Internal ID19146381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27541480hg38UCSC Ensembl
Innerchr19:27747981..28032388hg19UCSC Ensembl
Innerchr19:32439821..32724228hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38284408
hg19284408
hg18284408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3571974
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)nsv1057162
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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