A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963650



Internal ID22738585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3898545..3898545hg38UCSC Ensembl
chr10:3940737..3940737hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963650
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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