A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291721



Internal ID20500939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82510407..82510496hg38UCSC Ensembl
chr9:85125322..85125411hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291721
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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