A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039906



Internal ID21949249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38988200..38988397hg38UCSC Ensembl
chr13:39562337..39562534hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606120
Samples
Known GenesSTOML3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039906
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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