A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908323



Internal ID6346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90224257..90756135hg38UCSC Ensembl
chr1:90689815..91221692hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38531879
hg19531878
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563291
Supporting Variants
Samples
Known GenesBARHL2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908323
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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