A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003073



Internal ID21912416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98427322..98427504hg38UCSC Ensembl
chr7:98056634..98056816hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003073
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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