A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095281



Internal ID22004514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36624732..36624732hg38UCSC Ensembl
chr11:36646282..36646282hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587470
Samples
Known GenesC11orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095281
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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