A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909252



Internal ID6957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3448580..3448580hg38UCSC Ensembl
chr2:3452351..3452351hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547823
Supporting Variants
Samples
Known GenesTRAPPC12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909252
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.040669


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