A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939611



Internal ID27128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135740400..135741227hg38UCSC Ensembl
chr3:135459242..135460069hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939611
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer