A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959063



Internal ID22734108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60121856..60121856hg38UCSC Ensembl
chr1:60587528..60587528hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959063
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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