A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923964



Internal ID16737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223854369..223855241hg38UCSC Ensembl
chr2:224719086..224719958hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563644
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923964
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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