A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684400



Internal ID108066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109962116..109962261hg38UCSC Ensembl
chr12:110399921..110400066hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509728
Supporting Variants
Samples
Known GenesGIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684400
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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