A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065853



Internal ID19155072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39270288..39371087hg38UCSC Ensembl
Innerchr18:36850252..36951051hg19UCSC Ensembl
Innerchr18:35104250..35205049hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38100800
hg19100800
hg18100800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725318
Samples
Known GenesLINC00669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065853
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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