A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440542



Internal ID21098095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89084024..89108750hg38UCSC Ensembl
chr10:90843781..90868507hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3824727
hg1924727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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