A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918687



Internal ID22693909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6914472..6923602hg38UCSC Ensembl
chr10:6956434..6965564hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389131
hg199131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918687
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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