A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442084



Internal ID21099637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20225949..20325811hg38UCSC Ensembl
chr10:20514878..20614740hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3899863
hg1999863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193753
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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