A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446742



Internal ID21104295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94730074..94730740hg38UCSC Ensembl
chr10:96489831..96490497hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985294
Samples
Known GenesCYP2C18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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