A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046687



Internal ID19135906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43264654..43363017hg38UCSC Ensembl
Innerchr14:43733857..43832220hg19UCSC Ensembl
Innerchr14:42803607..42901970hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3898364
hg1998364
hg1898364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1889n100
Supporting Variantsnssv3530224
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)nsv1046687
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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