A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072040



Internal ID21981273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13363169..13363169hg38UCSC Ensembl
chr6:13363401..13363401hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg386058
hg196058
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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