A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110950



Internal ID21294216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:181889246..181892615hg38UCSC Ensembl
Innerchr2:182753973..182757342hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg383370
hg193370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105683
Samplessample208
Known GenesSSFA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110950
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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