A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025901



Internal ID21935244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30161158..30161225hg38UCSC Ensembl
chr13:30735295..30735362hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025901
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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