A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008431



Internal ID21917774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104974753..104975089hg38UCSC Ensembl
chr7:104615200..104615536hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008431
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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