A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044012



Internal ID19133231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:29948617..30000552hg38UCSC Ensembl
Innerchr14:30417823..30469758hg19UCSC Ensembl
Innerchr14:29487574..29539509hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3851936
hg1951936
hg1851936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528584
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)nsv1044012
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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