A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611073



Internal ID6651293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142064430..142082667hg38UCSC Ensembl
Innerchr6:142064430..142082667hg38UCSC Ensembl
Outerchr6:142064323..142082820hg38UCSC Ensembl
chr6:142385567..142403804hg19UCSC Ensembl
Innerchr6:142385567..142403804hg19UCSC Ensembl
Outerchr6:142385460..142403957hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3818238
hg1918238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12573592, essv12573591
SamplesHG03998, HG03873
Known GenesNMBR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611073
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer