A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910330



Internal ID22685541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39214490..39303309hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3888820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910330
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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