A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15182980



Internal ID21321776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106775337..106775389hg38UCSC Ensembl
chr13:107427685..107427737hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946926
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15182980
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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