A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983801



Internal ID20550841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72255218..72286619hg38UCSC Ensembl
chr10:74014976..74046377hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3831402
hg1931402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448516
Supporting Variants
Samples
Known GenesDDIT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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