A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048300



Internal ID100071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73110275..73110326hg38UCSC Ensembl
chr11:72821320..72821371hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5400069
Supporting Variants
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048300
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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