A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17056805



Internal ID105704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47360978..47361029hg38UCSC Ensembl
chr12:47754761..47754812hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17056805
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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