A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054303



Internal ID18796834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82551672..82792576hg38UCSC Ensembl
Innerchr14:83018016..83258920hg19UCSC Ensembl
Innerchr14:82087769..82328673hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38240905
hg19240905
hg18240905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713535
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054303
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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