A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1928n100



Internal ID20153544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66586328..66668429hg38UCSC Ensembl
chr14:67053046..67135147hg19UCSC Ensembl
chr14:66122799..66204900hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3882102
hg1982102
hg1882102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046627, nsv1048504, nsv1049050, nsv1046763, nsv1040770
Samples
Known GenesGPHN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1928n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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