A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919182



Internal ID22694404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70597301..70597501hg38UCSC Ensembl
chr10:72357057..72357257hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364000
Samples
Known GenesPRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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