A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086877



Internal ID21285397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140305935..140309077hg38UCSC Ensembl
Innerchr7:140005735..140008877hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383143
hg193143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110463
Supporting Variants
Samplessample373
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086877
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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