A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923070



Internal ID16138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210977463..211003251hg38UCSC Ensembl
chr2:211842187..211867975hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3825789
hg1925789
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923070
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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