A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449364



Internal ID21106917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11461601..11465700hg38UCSC Ensembl
chr10:11503600..11507699hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190789
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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