A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051147



Internal ID19140366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35944136..36093657hg38UCSC Ensembl
Innerchr14:36413342..36562863hg19UCSC Ensembl
Innerchr14:35483093..35632614hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38149522
hg19149522
hg18149522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528620
Samples
Known GenesLINC00609
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051147
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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