A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480142



Internal ID257652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120793878..120793967hg38UCSC Ensembl
chr9:123556156..123556245hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027111
Samples
Known GenesLOC100288842
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480142
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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