A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463835



Internal ID241724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177684500..177740662hg38UCSC Ensembl
chr5:177111501..177167663hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3856163
hg1956163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976832
Samples
Known GenesFAM153A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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