A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021348



Internal ID21930691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85126719..85126966hg38UCSC Ensembl
chr13:85700854..85701101hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613125
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021348
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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