A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983452



Internal ID20550492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76619119..76621063hg38UCSC Ensembl
chr10:78378877..78380821hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381945
hg191945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00229


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