A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444616



Internal ID21102169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97425501..97427100hg38UCSC Ensembl
chr10:99185258..99186857hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179161
Samples
Known GenesPGAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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