A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025658



Internal ID84840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92830929..92832663hg38UCSC Ensembl
chr9:95593211..95594945hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474961
Supporting Variants
Samples
Known GenesANKRD19P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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