A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091318



Internal ID21280464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54237351..54242967hg38UCSC Ensembl
Innerchr1:54703024..54708640hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385617
hg195617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110520
Supporting Variants
Samplessample299
Known GenesSSBP3, SSBP3-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091318
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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