A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1418e214



Internal ID22757312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127483634..127521565hg38UCSC Ensembl
chr8:128495879..128533810hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3837932
hg1937932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3618774, esv3618775
SamplesNA19435, HG03488, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1418e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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