A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904564



Internal ID3865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67634392..67641879hg38UCSC Ensembl
chr1:68100075..68107562hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387488
hg197488
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904564
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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