A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438351



Internal ID21095904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94375560..95464833hg38UCSC Ensembl
chr10:96135317..97224590hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381089274
hg191089274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195468
Samples
Known GenesC10orf129, CYP2C18, CYP2C19, CYP2C8, CYP2C9, HELLS, PDLIM1, SORBS1, TBC1D12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438351
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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