A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025872



Internal ID84985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96416834..96417072hg38UCSC Ensembl
chr9:99179116..99179354hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479513
Supporting Variants
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025872
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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