A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965488



Internal ID22740423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191211230..191211230hg38UCSC Ensembl
chr2:192075956..192075956hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965488
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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