A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940819



Internal ID27918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149217851..149222772hg38UCSC Ensembl
chr3:148935638..148940559hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384922
hg194922
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555704
Supporting Variants
Samples
Known GenesCP
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940819
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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