A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912581



Internal ID22687797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116433604..116433888hg38UCSC Ensembl
chr10:118193116..118193400hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356195
Samples
Known GenesPNLIPRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912581
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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