A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013346



Internal ID21922689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138650112..138676936hg38UCSC Ensembl
chr7:138334857..138361681hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3826825
hg1926825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575683
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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