A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286656



Internal ID20495874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135946768..135946823hg38UCSC Ensembl
chr8:136959011..136959066hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286656
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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