A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565431



Internal ID21757396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20350..20350hg38UCSC Ensembl
chr7:20350..20350hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565431
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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