A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518483



Internal ID21842842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168928941..168928941hg38UCSC Ensembl
chr1:168898179..168898179hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057955
Supporting Variants
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518483
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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