A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1877n100



Internal ID22787964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40049637..40147703hg38UCSC Ensembl
chr14:40518841..40616907hg19UCSC Ensembl
chr14:39588592..39686658hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3898067
hg1998067
hg1898067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051963, nsv1037101
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)dgv1877n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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