A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276476



Internal ID20485694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90467442..90467500hg38UCSC Ensembl
chr9:93229724..93229782hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736711
Supporting Variants
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276476
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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