A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059094



Internal ID18801625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40239470..40252328hg38UCSC Ensembl
Innerchr19:40745377..40758235hg19UCSC Ensembl
Innerchr19:45437217..45450075hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812859
hg1912859
hg1812859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568213, nssv3568214
Samples
Known GenesAKT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059094
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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