A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037641



Internal ID18780172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73950133..74108086hg38UCSC Ensembl
Innerchr14:74416836..74574789hg19UCSC Ensembl
Innerchr14:73486589..73644542hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38157954
hg19157954
hg18157954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1937n100
Supporting Variantsnssv3531156
Samples
Known GenesALDH6A1, CCDC176, COQ6, ENTPD5, FAM161B, LIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037641
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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