A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1937n100



Internal ID19012305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73950133..74115803hg38UCSC Ensembl
chr14:74416836..74582506hg19UCSC Ensembl
chr14:73486589..73652259hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38165671
hg19165671
hg18165671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049103, nsv1042026, nsv1053866, nsv1037641, nsv1046333
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)dgv1937n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer