A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678138



Internal ID9944243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98155667..98212370hg38UCSC Ensembl
Outerchr3:98155633..98212405hg38UCSC Ensembl
Innerchr3:97874511..97931214hg19UCSC Ensembl
Outerchr3:97874477..97931249hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3856773
hg1956773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv872e199
Supporting Variantsessv6059800, essv5974262, essv5518656, essv5815974, essv5619291, essv5779205, essv5776704, essv6242452, essv6336695, essv6382219
SamplesHG00650, HG01052, HG00261, HG00512, NA18560, NA20342, NA19070, NA19056, NA19682, HG00258
Known GenesOR5H15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678138
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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