A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941895



Internal ID28619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154997859..155063916hg38UCSC Ensembl
chr3:154715648..154781705hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3866058
hg1966058
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941895
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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