A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440360



Internal ID21097913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119214172..119226759hg38UCSC Ensembl
chr10:120973684..120986271hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3812588
hg1912588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194005
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440360
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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