A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031335



Internal ID21940678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38402479..38402598hg38UCSC Ensembl
chr13:38976616..38976735hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031335
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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