A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265554



Internal ID20474772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21915001..21915001hg38UCSC Ensembl
chr9:21915000..21915000hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265554
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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