A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097799



Internal ID22007032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20029340..20029340hg38UCSC Ensembl
chr11:20050886..20050886hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583315
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097799
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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