A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2109n100



Internal ID20153725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106364803..106877229hg38UCSC Ensembl
chr14:106820732..107285437hg19UCSC Ensembl
chr14:105891777..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38512427
hg19464706
hg18464706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046943, nsv1052837
Samples
Known GenesLINC00221
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2109n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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