A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927240



Internal ID22702468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15425875..15425956hg38UCSC Ensembl
chr10:15467874..15467955hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927240
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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