A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065117



Internal ID19154336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27578429hg38UCSC Ensembl
Innerchr19:27747981..28069337hg19UCSC Ensembl
Innerchr19:32439821..32761177hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38321357
hg19321357
hg18321357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3572012, nssv3572013, nssv3572011, nssv3572009, nssv3572010
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)nsv1065117
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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