A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15182924



Internal ID21321720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58470629..58470945hg38UCSC Ensembl
chr13:59044763..59045079hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926278
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15182924
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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