A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614866



Internal ID21806913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90900573..90900877hg38UCSC Ensembl
chr15:91443803..91444107hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031294
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614866
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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