A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045636



Internal ID98188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34443026..34443077hg38UCSC Ensembl
chr11:34464573..34464624hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408220
Supporting Variants
Samples
Known GenesCAT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045636
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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