A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555597



Internal ID328751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175821320..175824282hg38UCSC Ensembl
chr5:175248323..175251285hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg382963
hg192963
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978714
Samples
Known GenesCPLX2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555597
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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