A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668674



Internal ID9934779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133261035..133269918hg38UCSC Ensembl
Outerchr6:133260998..133269968hg38UCSC Ensembl
Innerchr6:133582173..133591056hg19UCSC Ensembl
Outerchr6:133582136..133591106hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg388971
hg198971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6297781
SamplesNA18571
Known GenesEYA4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668674
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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