A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095191



Internal ID22004424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75877718..75877718hg38UCSC Ensembl
chr11:75588762..75588762hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590032
Samples
Known GenesUVRAG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095191
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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