A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747928



Internal ID21388010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93282047..93286046hg38UCSC Ensembl
chr10:95041804..95045803hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431407
Supporting Variants
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747928
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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