A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487579



Internal ID264913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134166582..134166633hg38UCSC Ensembl
chr9:137031704..137031755hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487579
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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