A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195195



Internal ID20762235
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 StatusS
Merged Variantsnsv6448461
Supporting Variants
Samples
Known GenesADD3, ADD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195195
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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