A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603352



Internal ID21795399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42094284..42107020hg38UCSC Ensembl
chr13:42668420..42681156hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3812737
hg1912737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031988
Supporting Variants
Samples
Known GenesDGKH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603352
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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