A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917912



Internal ID22693133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63958545..63976293hg38UCSC Ensembl
chr10:65718305..65736053hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3817749
hg1917749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917912
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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