A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705533



Internal ID21377809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31440563..31440692hg38UCSC Ensembl
chr13:32014700..32014829hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390577
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705533
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.235632


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