A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448461



Internal ID21106014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110005001..110011900hg38UCSC Ensembl
chr10:111764759..111771658hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195195
Samples
Known GenesADD3, ADD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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