A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192016



Internal ID20759056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51558794..51569875hg38UCSC Ensembl
chr10:53318554..53329635hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3811082
hg1911082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438241
Supporting Variants
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192016
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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