A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066675



Internal ID19155894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33716662..33743652hg38UCSC Ensembl
Innerchr19:34207567..34234557hg19UCSC Ensembl
Innerchr19:38899407..38926397hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3826991
hg1926991
hg1826991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3514n100
Supporting Variantsnssv3566579
Samples
Known GenesCHST8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066675
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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