A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965882



Internal ID22740817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26817975..26817975hg38UCSC Ensembl
chr4:26819597..26819597hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965882
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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