A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039135



Internal ID21948478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87927695..87927887hg38UCSC Ensembl
chr11:87638587..87638779hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039135
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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