A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021916



Internal ID21931259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26982958..26983027hg38UCSC Ensembl
chr13:27557095..27557164hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021916
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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