A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898303



Internal ID173012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229194420..229233415hg38UCSC Ensembl
chr1:229330167..229369162hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3838996
hg1938996
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898303
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003122


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