A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029963



Internal ID87696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132126469..132126520hg38UCSC Ensembl
chr9:135001856..135001907hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029963
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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