A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451160



Internal ID21108713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87044719..87058168hg38UCSC Ensembl
chr10:88804476..88817925hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3813450
hg1913450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192010
Samples
Known GenesGLUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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