A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047054



Internal ID19136273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55455569..55568861hg38UCSC Ensembl
Innerchr14:55922287..56035579hg19UCSC Ensembl
Innerchr14:54992040..55105332hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38113293
hg19113293
hg18113293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531026
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)nsv1047054
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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