A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294657



Internal ID20503875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231472902..231472902hg38UCSC Ensembl
chr2:232337613..232337613hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294657
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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