A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090150



Internal ID5833297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35106972..35120339hg38UCSC Ensembl
Innerchr11:35106972..35120339hg38UCSC Ensembl
Outerchr11:35106472..35120839hg38UCSC Ensembl
chr11:35128519..35141886hg19UCSC Ensembl
Innerchr11:35128519..35141886hg19UCSC Ensembl
Outerchr11:35128019..35142386hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3813368
hg1913368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625921
Supporting Variants
SamplesNA19207
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090150
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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