A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960519



Internal ID22735492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9321047..9321047hg38UCSC Ensembl
chr10:9363010..9363010hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960519
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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