A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025870



Internal ID84983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96403972..96405059hg38UCSC Ensembl
chr9:99166254..99167341hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477826
Supporting Variants
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025870
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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