A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192946



Internal ID20759986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114822501..114827900hg38UCSC Ensembl
chr10:116582260..116587659hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452361
Supporting Variants
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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