A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431409



Internal ID21393411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93282057..93286046hg38UCSC Ensembl
chr10:95041814..95045803hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383990
hg193990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n172
Supporting Variantsnssv15746432
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431409
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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