A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983209



Internal ID20550249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59313547..59314048hg38UCSC Ensembl
chr10:61073307..61073808hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453939
Supporting Variants
Samples
Known GenesFAM13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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