A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579045



Internal ID21771088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97934390..97934457hg38UCSC Ensembl
chr9:100696672..100696739hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004825
Supporting Variants
Samples
Known GenesHEMGN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579045
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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