A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610089



Internal ID21802136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47788232..47790077hg38UCSC Ensembl
chr15:48080429..48082274hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381846
hg191846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610089
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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