A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028650



Internal ID21937993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100126314..100131112hg38UCSC Ensembl
chr13:100778568..100783366hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384799
hg194799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601121
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028650
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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