A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961853



Internal ID22736794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88103994..88103994hg38UCSC Ensembl
chr5:87399811..87399811hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961853
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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