A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596171



Internal ID21788214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37473232..37473304hg38UCSC Ensembl
chr9:37473229..37473301hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596171
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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