A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559920



Internal ID21884275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128386613..128386613hg38UCSC Ensembl
chr7:128026667..128026667hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559920
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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