A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260324



Internal ID20469542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98423190..98423710hg38UCSC Ensembl
chr7:98052502..98053022hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260324
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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