A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927079



Internal ID22702307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20820781..20880315hg38UCSC Ensembl
chr10:21109710..21169244hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3859535
hg1959535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365191
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927079
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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