A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13999995



Internal ID2920224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4901278..4903008hg38UCSC Ensembl
Innerchr11:4901281..4903005hg38UCSC Ensembl
Outerchr11:4901275..4903011hg38UCSC Ensembl
chr11:4922508..4924238hg19UCSC Ensembl
Innerchr11:4922511..4924235hg19UCSC Ensembl
Outerchr11:4922505..4924241hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381731
hg191731
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625197
Supporting Variants
SamplesHG02583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13999995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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