A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295870



Internal ID20505088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28228466..28228553hg38UCSC Ensembl
chr15:28473612..28473699hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750110
Supporting Variants
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295870
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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