A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027946



Internal ID86327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121752238..121752452hg38UCSC Ensembl
chr9:124514517..124514731hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484421
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027946
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.019201


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