A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280951



Internal ID20490169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111545638..111545726hg38UCSC Ensembl
chr13:112197985..112198073hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280951
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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