A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1197e214



Internal ID22757091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82810467..82865064hg38UCSC Ensembl
chr6:83520186..83574783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3854598
hg1954598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3609768, esv3609767
SamplesNA12399, NA19031, NA20282
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1197e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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