A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578726



Internal ID16019449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669207..15724712hg38UCSC Ensembl
Innerchr19:15780017..15835522hg19UCSC Ensembl
Innerchr19:15641017..15696522hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3855506
hg1955506
hg1855506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n54
Supporting Variantsnssv1149843, nssv1149841, nssv1149842
SamplesHGDP00942, HGDP00459, HGDP00450
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578726
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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