A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317792



Internal ID4319608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132851178..132855786hg38UCSC Ensembl
Innerchr11:132851197..132855767hg38UCSC Ensembl
Outerchr11:132851159..132855805hg38UCSC Ensembl
chr11:132721073..132725681hg19UCSC Ensembl
Innerchr11:132721092..132725662hg19UCSC Ensembl
Outerchr11:132721054..132725700hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384609
hg194609
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628133
Supporting Variants
SamplesNA18951
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317792
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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