A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983211



Internal ID20550251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59331399..59332027hg38UCSC Ensembl
chr10:61091159..61091787hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450055
Supporting Variants
Samples
Known GenesFAM13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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