A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3572029



Internal ID18870310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27636744hg38UCSC Ensembl
Innerchr19:27747981..28127652hg19UCSC Ensembl
Innerchr19:32439821..32819492hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38379672
hg19379672
hg18379672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060114
Supporting Variants
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)nssv3572029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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