A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604282



Internal ID21796329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28228484..28228568hg38UCSC Ensembl
chr15:28473630..28473714hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039539
Supporting Variants
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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