A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14080053



Internal ID2739071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32327012..32327951hg38UCSC Ensembl
Innerchr11:32327034..32327930hg38UCSC Ensembl
Outerchr11:32326991..32327973hg38UCSC Ensembl
chr11:32348558..32349497hg19UCSC Ensembl
Innerchr11:32348580..32349476hg19UCSC Ensembl
Outerchr11:32348537..32349519hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625857
Supporting Variants
SamplesHG02407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14080053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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