A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843313



Internal ID22026956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119089653..119089653hg38UCSC Ensembl
chr11:118960363..118960363hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258396
Supporting Variants
Samples
Known GenesHMBS
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843313
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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