A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17984372



Internal ID20551412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78577920..78580586hg38UCSC Ensembl
chr10:80337677..80340343hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382667
hg192667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17984372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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