A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066992



Internal ID18809523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15683785..15714929hg38UCSC Ensembl
Innerchr19:15794595..15825739hg19UCSC Ensembl
Innerchr19:15655595..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3831145
hg1931145
hg1831145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3452n100
Supporting Variantsnssv3569770, nssv3569776, nssv3569774, nssv3569772, nssv3569773, nssv3569771, nssv3569775
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066992
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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