A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272562



Internal ID20481780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36254781..36254851hg38UCSC Ensembl
chr9:36254778..36254848hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732447
Supporting Variants
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272562
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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