A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608404



Internal ID21800451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94244294..94244294hg38UCSC Ensembl
chr15:94787523..94787523hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608404
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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