A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066596



Internal ID19155815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40846466..40875029hg38UCSC Ensembl
Innerchr19:41352371..41380934hg19UCSC Ensembl
Innerchr19:46044211..46072774hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3828564
hg1928564
hg1828564
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3536n100
Supporting Variantsnssv3569418, nssv3569416, nssv3569423, nssv3569419, nssv3569424, nssv3569425, nssv3569415, nssv3569422, nssv3569421, nssv3569417, nssv3569420
Samples
Known GenesCYP2A6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066596
Frequency
Sample Size11257
Observed Gain5
Observed Loss6
Observed Complex0
Frequencyn/a


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