A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484357



Internal ID261769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127452036..127452437hg38UCSC Ensembl
chr9:130214315..130214716hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028776
Samples
Known GenesLRSAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484357
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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