A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910041



Internal ID22685251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82106153..82106217hg38UCSC Ensembl
chr10:83865909..83865973hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364249
Samples
Known GenesNRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910041
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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