A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983069



Internal ID20550109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69451901..69455400hg38UCSC Ensembl
chr10:71211657..71215156hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454965
Supporting Variants
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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