A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559776



Internal ID332799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146100825..146100825hg38UCSC Ensembl
chr5:145480388..145480388hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974635
Samples
Known GenesPLAC8L1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559776
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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