A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454783



Internal ID21112336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72230782..72231433hg38UCSC Ensembl
chr10:73990540..73991191hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184703
Samples
Known GenesANAPC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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