A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031128



Internal ID21940471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44277359..44277457hg38UCSC Ensembl
chr13:44851495..44851593hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031128
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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