A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920820



Internal ID22696043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273310..9273466hg38UCSC Ensembl
chr10:9315273..9315429hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920820
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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