A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956781



Internal ID22731937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89128356..89128356hg38UCSC Ensembl
chr1:89594039..89594039hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956781
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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