A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054457



Internal ID19143676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38644977..38848279hg38UCSC Ensembl
Innerchr14:39114181..39317483hg19UCSC Ensembl
Innerchr14:38183932..38387234hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38203303
hg19203303
hg18203303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712287
Samples
Known GenesLINC00639
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054457
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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