A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027968



Internal ID21937311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31486886..31487067hg38UCSC Ensembl
chr13:32061023..32061204hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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