A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979296



Internal ID20546336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25338484..25353095hg38UCSC Ensembl
chr10:25627413..25642024hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3814612
hg1914612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450306
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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