A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558556



Internal ID21882911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99803111..99804508hg38UCSC Ensembl
chr7:99400734..99402131hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558556
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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