A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064734



Internal ID18807265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42571894..42678326hg38UCSC Ensembl
Innerchr19:43076046..43182478hg19UCSC Ensembl
Innerchr19:47767886..47874318hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38106433
hg19106433
hg18106433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568650
Samples
Known GenesCEACAM8, LIPE-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064734
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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