A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14097580



Internal ID4099396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38831875..38940297hg38UCSC Ensembl
Innerchr11:38831908..38940264hg38UCSC Ensembl
Outerchr11:38831842..38940330hg38UCSC Ensembl
chr11:38853425..38961847hg19UCSC Ensembl
Innerchr11:38853458..38961814hg19UCSC Ensembl
Outerchr11:38853392..38961880hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38108423
hg19108423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626021
Supporting Variants
SamplesNA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14097580
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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