A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191314



Internal ID20758354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47746501..47750400hg38UCSC Ensembl
chr10:46954295..46958195hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383900
hg193901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443563
Supporting Variants
Samples
Known GenesSYT15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02636


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