A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983594



Internal ID20550634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79450817..79454691hg38UCSC Ensembl
chr10:81210573..81214447hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383875
hg193875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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