A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588987



Internal ID21781030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52561143..52561143hg38UCSC Ensembl
chr10:54320903..54320903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588987
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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