A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554177



Internal ID327373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172832319..172839154hg38UCSC Ensembl
chr5:172259322..172266157hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386836
hg196836
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978628
Samples
Known GenesERGIC1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554177
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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