A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1208e214



Internal ID22757102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106713127..106725941hg38UCSC Ensembl
chr6:107161002..107173816hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3812815
hg1912815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3610284, esv3610285
SamplesHG00242, HG02624, HG00150, HG01134, HG00266, HG00625
Known GenesLOC100422737
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1208e214
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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