A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034438



Internal ID21943781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99583891..99586089hg38UCSC Ensembl
chr13:100236145..100238343hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382199
hg192199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034438
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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