A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960726



Internal ID22735693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86925694..86925694hg38UCSC Ensembl
chr10:88685451..88685451hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960726
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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