A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670783



Internal ID9590202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11059326..11087887hg38UCSC Ensembl
chr6:11059559..11088120hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3828562
hg1928562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5663764, essv5467186
SamplesNA18530, NA18542
Known GenesELOVL2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670783
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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