A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571976



Internal ID18870257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27543810hg38UCSC Ensembl
Innerchr19:27747981..28034718hg19UCSC Ensembl
Innerchr19:32439821..32726558hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38286738
hg19286738
hg18286738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066189
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)nssv3571976
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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