A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596602



Internal ID21788645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28048858..28049606hg38UCSC Ensembl
chr9:28048856..28049604hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003643
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596602
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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