A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445744



Internal ID21103297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68896575..68942756hg38UCSC Ensembl
chr10:70656331..70702512hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3846182
hg1946182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179426
Samples
Known GenesDDX50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445744
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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