A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492106



Internal ID269327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13787045..13822799hg38UCSC Ensembl
chr9:13787044..13822798hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3835755
hg1935755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492106
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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