A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438212



Internal ID21095765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111582201..111592700hg38UCSC Ensembl
chr10:113341959..113352458hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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