A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066251



Internal ID19155470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27672540hg38UCSC Ensembl
Innerchr19:27747981..28163448hg19UCSC Ensembl
Innerchr19:32439821..32855288hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38415468
hg19415468
hg18415468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3499n100
Supporting Variantsnssv3572033, nssv3572034
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)nsv1066251
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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