A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284629



Internal ID20493847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83009063..83011287hg38UCSC Ensembl
chr15:83677815..83680039hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382225
hg192225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749005
Supporting Variants
Samples
Known GenesC15orf40
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284629
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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