A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105004



Internal ID21267234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25533642..25552032hg38UCSC Ensembl
Innerchr2:25756511..25774901hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3818391
hg1918391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116239
Supporting Variants
Samplessample11
Known GenesDTNB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105004
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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