A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970675



Internal ID47777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96147326..96274352hg38UCSC Ensembl
chr5:95483030..95610056hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38127027
hg19127027
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970675
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001249


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