A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181256



Internal ID20748296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5410601..5415700hg38UCSC Ensembl
chr10:5452564..5457663hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436306
Supporting Variants
Samples
Known GenesNET1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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