A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922399



Internal ID15693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175818482..175819882hg38UCSC Ensembl
chr2:176683210..176684610hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922399
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004527


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