A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115136



Internal ID21298402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:146990724..146994379hg38UCSC Ensembl
Innerchr6:147311860..147315515hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg383656
hg193656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083685
Samplessample58
Known GenesSTXBP5-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115136
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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