A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181629



Internal ID20748669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51537991..52321749hg38UCSC Ensembl
chr10:53297751..54081509hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38783759
hg19783759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441234
Supporting Variants
Samples
Known GenesCSTF2T, DKK1, PRKG1, PRKG1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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