A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105687



Internal ID21290001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28213142..28235679hg38UCSC Ensembl
Innerchr1:28539653..28562190hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3822538
hg1922538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116922
Supporting Variants
Samplessample54
Known GenesDNAJC8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105687
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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