A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439563



Internal ID21097116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118046501..118048100hg38UCSC Ensembl
chr10:119806012..119807611hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179118
Samples
Known GenesCASC2, RAB11FIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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