A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487531



Internal ID264865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92831657..92831916hg38UCSC Ensembl
chr9:95593939..95594198hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025659
Samples
Known GenesANKRD19P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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