A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600443



Internal ID21792490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72513789..72513789hg38UCSC Ensembl
chr15:72806130..72806130hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094166
Supporting Variants
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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