A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894286



Internal ID170348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189885472..190021353hg38UCSC Ensembl
chr1:189854602..189990483hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38135882
hg19135882
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894286
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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