A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564110



Internal ID21888465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52940230..52940230hg38UCSC Ensembl
chr6:52805028..52805028hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564110
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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