A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438388



Internal ID21095941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97439007..97440227hg38UCSC Ensembl
chr10:99198764..99199984hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183815
Samples
Known GenesEXOSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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