A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261291



Internal ID20470509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99903537..99903537hg38UCSC Ensembl
chr9:102665819..102665819hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764653
Supporting Variants
Samples
Known GenesLOC441461
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261291
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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