A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954471



Internal ID22729709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214604450..214604450hg38UCSC Ensembl
chr2:215469174..215469174hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954471
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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