A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv389e214



Internal ID22756283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27541361..27625731hg38UCSC Ensembl
chr14:28010567..28094937hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3884371
hg1984371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633881, esv3633880
SamplesHG02628, HG01565, HG04019, HG04200, HG01566
Known GenesLINC00645
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv389e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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