A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243589



Internal ID6181267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95540524..95552110hg38UCSC Ensembl
Innerchr11:95540533..95552101hg38UCSC Ensembl
Outerchr11:95540515..95552119hg38UCSC Ensembl
chr11:95273688..95285274hg19UCSC Ensembl
Innerchr11:95273697..95285265hg19UCSC Ensembl
Outerchr11:95273679..95285283hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811587
hg1911587
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627355
Supporting Variants
SamplesNA19717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243589
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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