A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610321



Internal ID6997238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108466433..108471496hg38UCSC Ensembl
Innerchr6:108466449..108471480hg38UCSC Ensembl
Outerchr6:108466417..108471512hg38UCSC Ensembl
chr6:108787636..108792699hg19UCSC Ensembl
Innerchr6:108787652..108792683hg19UCSC Ensembl
Outerchr6:108787620..108792715hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385064
hg195064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499620
SamplesHG03756
Known GenesLACE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610321
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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