A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276949



Internal ID20486167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232793044..232793044hg38UCSC Ensembl
chr1:232928790..232928790hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276949
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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