A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985988



Internal ID20553028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97302826..97305124hg38UCSC Ensembl
chr10:99062583..99064881hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382299
hg192299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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