A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364384



Internal ID22590053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102556626..102556971hg38UCSC Ensembl
chr10:104316383..104316728hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908399
Supporting Variants
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364384
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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