A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980373



Internal ID20547413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44808301..44811600hg38UCSC Ensembl
chr10:45303749..45307048hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450006
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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