A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597224



Internal ID21789267
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 StatusS
Merged Variantsnsv6094399
Supporting Variants
Samples
Known GenesLOC283214
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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