A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962642



Internal ID22737577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43417020..43417020hg38UCSC Ensembl
chr10:43912468..43912468hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962642
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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