A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020029



Internal ID21929372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155594372..155594453hg38UCSC Ensembl
chr7:155387066..155387147hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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