A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282697



Internal ID20491915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42181823..42182095hg38UCSC Ensembl
chr13:42755959..42756231hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743744
Supporting Variants
Samples
Known GenesDGKH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282697
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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