A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088584



Internal ID21274563
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 StatusS
Merged Variantsnsv3110993
Supporting Variants
Samplessample208
Known GenesTM9SF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088584
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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