A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440568



Internal ID21098121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102154928..102157716hg38UCSC Ensembl
chr10:103914685..103917473hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg382789
hg192789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977244
Samples
Known GenesNOLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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