A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032612



Internal ID21941955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86889414..86989786hg38UCSC Ensembl
chr13:87541669..87642041hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38100373
hg19100373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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