A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196927



Internal ID20763967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56352901..56357400hg38UCSC Ensembl
chr10:58112662..58117161hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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