A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611359



Internal ID6998268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156744326..156758046hg38UCSC Ensembl
Innerchr6:156744826..156757546hg38UCSC Ensembl
Outerchr6:156743326..156759046hg38UCSC Ensembl
chr6:157065460..157079180hg19UCSC Ensembl
Innerchr6:157065960..157078680hg19UCSC Ensembl
Outerchr6:157064460..157080180hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3813721
hg1913721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1230e214
Supporting Variantsessv12601090
SamplesNA18616
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611359
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