A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442326



Internal ID21099879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82362050..82382401hg38UCSC Ensembl
chr10:84121806..84142157hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820352
hg1920352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984154
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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