A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187814



Internal ID20754854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114754148..114762329hg38UCSC Ensembl
chr10:116513907..116522088hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg388182
hg198182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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