A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053842



Internal ID103732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131980211..131980262hg38UCSC Ensembl
chr11:131850105..131850156hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430161
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053842
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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