A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438075



Internal ID21095628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115904466..115915602hg38UCSC Ensembl
chr10:117663977..117675113hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811137
hg1911137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977480
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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