A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14009044



Internal ID4482482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6170391..6185596hg38UCSC Ensembl
Innerchr11:6170391..6185596hg38UCSC Ensembl
Outerchr11:6169891..6186096hg38UCSC Ensembl
chr11:6191621..6206826hg19UCSC Ensembl
Innerchr11:6191621..6206826hg19UCSC Ensembl
Outerchr11:6191121..6207326hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815206
hg1915206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625263
Supporting Variants
SamplesHG03985
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14009044
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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