A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583275



Internal ID21775318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126410628..126410628hg38UCSC Ensembl
chr10:128099197..128099197hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583275
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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