A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1227e214



Internal ID22757121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142796373..142806407hg38UCSC Ensembl
chr6:143117510..143127544hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3810035
hg1910035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611083, esv3611082
SamplesHG00693, NA19917, NA19725, HG00628
Known GenesHIVEP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1227e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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