A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030030



Internal ID87737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132988756..132989000hg38UCSC Ensembl
chr9:135864143..135864387hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492531
Supporting Variants
Samples
Known GenesGFI1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030030
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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