A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020367



Internal ID21929710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14990180..15021404hg38UCSC Ensembl
chr7:15029805..15061029hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3831225
hg1931225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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