A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486947



Internal ID264297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81795235..81805414hg38UCSC Ensembl
chr9:84410150..84420329hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3810180
hg1910180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486947
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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