A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753106



Internal ID21389469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93282047..93286048hg38UCSC Ensembl
chr10:95041804..95045805hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384002
hg194002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431408
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753106
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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