A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927279



Internal ID18899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173632750..173632750hg38UCSC Ensembl
chr2:174497478..174497478hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927279
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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