A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087665



Internal ID21274569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131133184..131136794hg38UCSC Ensembl
Innerchr6:131454324..131457934hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383611
hg193611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114620
Supporting Variants
Samplessample208
Known GenesAKAP7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087665
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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