A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961883



Internal ID22736824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107255432..107255432hg38UCSC Ensembl
chr5:106591133..106591133hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961883
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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