A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275238



Internal ID20484456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30839244..30839597hg38UCSC Ensembl
chr13:31413381..31413734hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275238
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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