A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541801



Internal ID21866156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183449702..183449702hg38UCSC Ensembl
chr3:183167490..183167490hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074617
Supporting Variants
Samples
Known GenesLINC00888
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541801
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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