A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044986



Internal ID97739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44077163..44077214hg38UCSC Ensembl
chr11:44098713..44098764hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410129
Supporting Variants
Samples
Known GenesACCS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044986
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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