A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099068



Internal ID22008301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881502..881502hg38UCSC Ensembl
chr11:881502..881502hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596103
Samples
Known GenesCHID1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099068
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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