A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900882



Internal ID1387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2536162..2536162hg38UCSC Ensembl
chr2:2539934..2539934hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.477614


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