A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv678e214



Internal ID22756572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14338129..14485856hg38UCSC Ensembl
chr2:14478253..14625980hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38147728
hg19147728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3589882, esv3589883
SamplesHG03790, NA20790
Known GenesLINC00276
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv678e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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