A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1876n100



Internal ID22787963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39891162..39964218hg38UCSC Ensembl
chr14:40360366..40433422hg19UCSC Ensembl
chr14:39430117..39503173hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3873057
hg1973057
hg1873057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035957, nsv1048773, nsv1050737
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)dgv1876n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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