A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046943



Internal ID18789474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106447150..106877229hg38UCSC Ensembl
Innerchr14:106903056..107285437hg19UCSC Ensembl
Innerchr14:105974101..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38430080
hg19382382
hg18382382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2109n100
Supporting Variantsnssv3714421
Samples
Known GenesLINC00221
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046943
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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