A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961708



Internal ID41772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1583098..1583438hg38UCSC Ensembl
chr5:1583213..1583553hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561188
Supporting Variants
Samples
Known GenesSDHAP3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961708
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.037309


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