A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193731



Internal ID20760771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51844996..52464544hg38UCSC Ensembl
chr10:53604756..54224304hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38619549
hg19619549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446525
Supporting Variants
Samples
Known GenesDKK1, PRKG1, PRKG1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193731
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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