A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917334



Internal ID22692553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43992911..44010709hg38UCSC Ensembl
chr10:44488359..44506157hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3817799
hg1917799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917334
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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