A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448643



Internal ID21106196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122873901..122883400hg38UCSC Ensembl
chr10:124633417..124642916hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178607
Samples
Known GenesFAM24B, FAM24B-CUZD1, LOC399815
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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