A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181616



Internal ID20748656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117535309..117887959hg38UCSC Ensembl
chr10:119294820..119647470hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38352651
hg19352651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443595
Supporting Variants
Samples
Known GenesEMX2, EMX2OS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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