A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1963n100



Internal ID22788050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94418982..94445260hg38UCSC Ensembl
chr14:94885319..94911597hg19UCSC Ensembl
chr14:93955072..93981350hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3826279
hg1926279
hg1826279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049959, nsv1035985, nsv1038227, nsv1051847, nsv1044036
Samples
Known GenesSERPINA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1963n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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