A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450116



Internal ID21107669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92460012..92460997hg38UCSC Ensembl
chr10:94219769..94220754hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985425
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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