A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442026



Internal ID21099579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103522378..103527949hg38UCSC Ensembl
chr10:105282135..105287706hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977705
Samples
Known GenesNEURL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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