A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055457



Internal ID18797988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32075015..32097408hg38UCSC Ensembl
Innerchr18:29654978..29677371hg19UCSC Ensembl
Innerchr18:27908976..27931369hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3822394
hg1922394
hg1822394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564169
Samples
Known GenesRNF138
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055457
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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