A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561188



Internal ID334174
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 StatusM
Merged Variants
Supporting Variantsnssv16961708
Samples
Known GenesSDHAP3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561188
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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