A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449545



Internal ID21107098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22000401..22007200hg38UCSC Ensembl
chr10:22289330..22296129hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186398
Samples
Known GenesDNAJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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