A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967406



Internal ID22742341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21113290..21113290hg38UCSC Ensembl
chr10:21402219..21402219hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356467
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967406
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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