A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611009



Internal ID6997920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140405783..140450908hg38UCSC Ensembl
Innerchr6:140405783..140450908hg38UCSC Ensembl
Outerchr6:140405283..140451408hg38UCSC Ensembl
chr6:140726920..140772045hg19UCSC Ensembl
Innerchr6:140726920..140772045hg19UCSC Ensembl
Outerchr6:140726420..140772545hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3845126
hg1945126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12568549, essv12568550
SamplesHG03914, NA19759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611009
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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