A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091187



Internal ID21278733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4677956..4680782hg38UCSC Ensembl
Innerchr1:4738016..4740842hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117352
Supporting Variants
Samplessample273
Known GenesAJAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091187
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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