A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035022



Internal ID21944365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50402285..50404085hg38UCSC Ensembl
chr13:50976421..50978221hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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