A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283020



Internal ID20492238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74990978..74991101hg38UCSC Ensembl
chr15:75283319..75283442hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283020
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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