A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973756



Internal ID22748691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116433114..116433114hg38UCSC Ensembl
chr10:118192626..118192626hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352646
Samples
Known GenesPNLIPRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973756
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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