A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065285



Internal ID19154504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31947921..32035023hg38UCSC Ensembl
Innerchr18:29527884..29614986hg19UCSC Ensembl
Innerchr18:27781882..27868984hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3887103
hg1987103
hg1887103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564165
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)nsv1065285
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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