A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025414



Internal ID21934757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111905434..111905490hg38UCSC Ensembl
chr13:112559748..112559804hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025414
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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