A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984593



Internal ID20551633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8438944..8448476hg38UCSC Ensembl
chr10:8480907..8490439hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389533
hg199533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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