A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113618



Internal ID21296884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16014893..16054460hg38UCSC Ensembl
Innerchr1:16341388..16380955hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3839568
hg1939568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096558
Samplessample363
Known GenesCLCNKA, CLCNKB, HSPB7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113618
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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