A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010052



Internal ID21919395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:434592..434729hg38UCSC Ensembl
chr7:474575..474712hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010052
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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