A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454121



Internal ID21111674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68885823..68891816hg38UCSC Ensembl
chr10:70645579..70651572hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385994
hg195994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983053
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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