A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673138



Internal ID9939243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107365290..107374496hg38UCSC Ensembl
Outerchr11:107364919..107374866hg38UCSC Ensembl
Innerchr11:107236016..107245222hg19UCSC Ensembl
Outerchr11:107235645..107245592hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389948
hg199948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv239e199
Supporting Variantsessv6423118, essv5840139, essv5460443, essv5678396, essv5864294, essv5419498, essv6490776, essv5589844, essv5793222, essv5823674, essv6522401, essv5736897, essv6448221, essv6127575, essv6222299, essv6264735, essv5846826, essv6532820, essv6564512, essv6289574, essv5540482, essv5672157
SamplesHG01098, HG00640, HG00737, HG01070, HG01168, HG00736, HG01069, HG01080, HG01170, HG01176, HG01048, HG01183, HG01171, HG00732, HG01102, HG01197, HG01182, HG01101, HG01108, HG01082, HG01191, HG00553
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673138
Frequency
Sample Size1151
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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