A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14120107



Internal ID3636556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47199006..47211062hg38UCSC Ensembl
Innerchr11:47199006..47211062hg38UCSC Ensembl
Outerchr11:47198506..47211562hg38UCSC Ensembl
chr11:47220557..47232613hg19UCSC Ensembl
Innerchr11:47220557..47232613hg19UCSC Ensembl
Outerchr11:47220057..47233113hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3812057
hg1912057
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626198
Supporting Variants
SamplesHG03235
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14120107
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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