A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889324



Internal ID166977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115576584..115577911hg38UCSC Ensembl
chr1:116119205..116120532hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889324
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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