A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601402



Internal ID21793449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323280..81323355hg38UCSC Ensembl
chr15:81615621..81615696hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027516
Supporting Variants
Samples
Known GenesSTARD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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