A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611317



Internal ID6998226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154357566..154360435hg38UCSC Ensembl
Innerchr6:154357579..154360423hg38UCSC Ensembl
Outerchr6:154357554..154360448hg38UCSC Ensembl
chr6:154678700..154681569hg19UCSC Ensembl
Innerchr6:154678713..154681557hg19UCSC Ensembl
Outerchr6:154678688..154681582hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382870
hg192870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12593092
SamplesHG00622
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611317
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