A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv772e214



Internal ID22756666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3495458..3505403hg38UCSC Ensembl
chr20:3476105..3486050hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg389946
hg199946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3645041, esv3645042
SamplesNA19449, HG03084
Known GenesATRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv772e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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