A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563596



Internal ID21887951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:528804..528804hg38UCSC Ensembl
chr7:568441..568441hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563596
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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