A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589396



Internal ID21781439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97984693..97984759hg38UCSC Ensembl
chr9:100746975..100747041hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014228
Supporting Variants
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589396
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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