A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899331



Internal ID329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3368479..3534951hg38UCSC Ensembl
chr2:3372250..3582541hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38166473
hg19210292
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559561
Supporting Variants
Samples
Known GenesADI1, TRAPPC12, TSSC1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899331
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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