A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035356



Internal ID21944699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75566770..75675112hg38UCSC Ensembl
chr13:76140906..76249248hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38108343
hg19108343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612670
Samples
Known GenesLMO7, UCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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