A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586082



Internal ID21778125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82749654..82770061hg38UCSC Ensembl
chr10:84509410..84529817hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820408
hg1920408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006440
Supporting Variants
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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