A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065098



Internal ID19154317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27579279hg38UCSC Ensembl
Innerchr19:27747981..28070187hg19UCSC Ensembl
Innerchr19:32439821..32762027hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38322207
hg19322207
hg18322207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3572014, nssv3572015
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)nsv1065098
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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