A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579396



Internal ID21771439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121283153..121283229hg38UCSC Ensembl
chr9:124045431..124045507hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004341
Supporting Variants
Samples
Known GenesGSN, GSN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579396
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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