A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296635



Internal ID20505853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81461821..81461964hg38UCSC Ensembl
chr9:84076736..84076879hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740602
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296635
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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