A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087809



Internal ID21277082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149865458..149870464hg38UCSC Ensembl
Innerchr6:150186594..150191600hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385007
hg195007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111044
Supporting Variants
Samplessample245
Known GenesRAET1E-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087809
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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