A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564168



Internal ID18862449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32029972..32084565hg38UCSC Ensembl
Innerchr18:29609935..29664528hg19UCSC Ensembl
Innerchr18:27863933..27918526hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3854594
hg1954594
hg1854594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061305
Supporting Variants
Samples
Known GenesRNF125
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564168
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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