A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095325



Internal ID21282380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28399908..28407431hg38UCSC Ensembl
Innerchr1:28726419..28733942hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg387524
hg197524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113310
Supporting Variants
Samplessample325
Known GenesPHACTR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095325
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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