A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270768



Internal ID20479986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80228637..80234480hg38UCSC Ensembl
chr15:80520979..80526822hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385844
hg195844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270768
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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