A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110993



Internal ID21294259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96585595..96588738hg38UCSC Ensembl
Innerchr10:98345352..98348495hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv173n145
Supporting Variantsnssv14088584
Samplessample208
Known GenesTM9SF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110993
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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