A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1189e214



Internal ID20122612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61471934..61546621hg38UCSC Ensembl
chr6:62181839..62256526hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3874688
hg1974688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3609202, esv3609201
SamplesHG01031, HG02048, HG02086, HG01801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1189e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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