A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490004



Internal ID267268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95571594..95578907hg38UCSC Ensembl
chr9:98333876..98341189hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387314
hg197314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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