A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv419e214



Internal ID22756313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711659..98730148hg38UCSC Ensembl
chr14:99177996..99196485hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818490
hg1918490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3635470, esv3635471
SamplesHG01066, NA20752, HG01325, HG01064, NA20811, HG00250, HG01697, HG01631
Known GenesC14orf177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv419e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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