A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065587



Internal ID19154806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32700348..32726118hg38UCSC Ensembl
Innerchr18:30280311..30306081hg19UCSC Ensembl
Innerchr18:28534309..28560079hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3825771
hg1925771
hg1825771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3331n100
Supporting Variantsnssv3564177, nssv3564178
Samples
Known GenesKLHL14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065587
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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