A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243542



Internal ID3903431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95442258..95448343hg38UCSC Ensembl
Innerchr11:95442258..95448343hg38UCSC Ensembl
Outerchr11:95441758..95448843hg38UCSC Ensembl
chr11:95175422..95181507hg19UCSC Ensembl
Innerchr11:95175422..95181507hg19UCSC Ensembl
Outerchr11:95174922..95182007hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627350
Supporting Variants
SamplesHG03558
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243542
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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