A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974351



Internal ID50270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133315069..133320360hg38UCSC Ensembl
chr5:132650761..132656052hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg385292
hg195292
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562128
Supporting Variants
Samples
Known GenesFSTL4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974351
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001093


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