A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922108



Internal ID22697333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82362045..82382400hg38UCSC Ensembl
chr10:84121801..84142156hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820356
hg1920356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353720
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922108
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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