A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196681



Internal ID20763721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19679535..20439070hg38UCSC Ensembl
chr10:19968464..20727999hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38759536
hg19759536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442321
Supporting Variants
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196681
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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