A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025714



Internal ID21935057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112150881..112150986hg38UCSC Ensembl
chr13:112805195..112805300hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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