A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6456212



Internal ID9785303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46948543..46949117hg38UCSC Ensembl
Outerchr11:46948386..46949270hg38UCSC Ensembl
Innerchr11:46970094..46970668hg19UCSC Ensembl
Outerchr11:46969937..46970821hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675104
Supporting Variants
SamplesNA19776
Known GenesC11orf49
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6456212
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