A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290693



Internal ID20499911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58254406..58254466hg38UCSC Ensembl
chr8:59166965..59167025hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290693
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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