A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186023



Internal ID20753063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63522001..63525900hg38UCSC Ensembl
chr10:65281761..65285660hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443012
Supporting Variants
Samples
Known GenesREEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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