A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560351



Internal ID21884706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98430972..98431548hg38UCSC Ensembl
chr7:98060284..98060860hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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