A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437285



Internal ID21094838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115307027..115447685hg38UCSC Ensembl
chr10:117066537..117207195hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38140659
hg19140659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977938
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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