A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582526



Internal ID21774569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2722407..2722472hg38UCSC Ensembl
chr9:2722407..2722472hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015957
Supporting Variants
Samples
Known GenesKCNV2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582526
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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