A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924749



Internal ID17243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207223645..207231407hg38UCSC Ensembl
chr2:208088369..208096131hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg387763
hg197763
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924749
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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