A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958775



Internal ID22733834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18982112..18982112hg38UCSC Ensembl
chr1:19308606..19308606hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958775
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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