A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094399



Internal ID22003632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763434..75763434hg38UCSC Ensembl
chr11:75474479..75474479hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597224
Samples
Known GenesLOC283214
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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