A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579986



Internal ID21772029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126530592..126530592hg38UCSC Ensembl
chr10:128219161..128219161hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086874
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579986
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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