A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062693



Internal ID19151912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75062572..75138621hg38UCSC Ensembl
Innerchr18:72774528..72850576hg19UCSC Ensembl
Innerchr18:70903516..70979564hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3876050
hg1976049
hg1876049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563027
Samples
Known GenesZNF407
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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