A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055091



Internal ID104562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7176244..7176289hg38UCSC Ensembl
chr12:7328840..7328885hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014049


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