A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040105



Internal ID19129324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46452735..46528955hg38UCSC Ensembl
Innerchr14:46921938..46998158hg19UCSC Ensembl
Innerchr14:45991688..46067908hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3876221
hg1976221
hg1876221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531671
Samples
Known GenesLINC00871
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040105
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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