A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058606



Internal ID18801137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:80023442..80257174hg38UCSC Ensembl
Innerchr18:77783442..78015057hg19UCSC Ensembl
Innerchr18:75884430..76116029hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38233733
hg19231616
hg18231600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3413n100
Supporting Variantsnssv3563070
Samples
Known GenesADNP2, PARD6G, PARD6G-AS1, RBFA, RBFADN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058606
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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