A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102387



Internal ID21285848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:70753940..70764342hg38UCSC Ensembl
Innerchr2:70981072..70991474hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3810403
hg1910403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118175
Supporting Variants
Samplessample38
Known GenesADD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102387
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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