A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968274



Internal ID46165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65138471..65139990hg38UCSC Ensembl
chr5:64434298..64435817hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968274
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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