A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083588



Internal ID21270931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87330427..87331309hg38UCSC Ensembl
Innerchr1:87796110..87796992hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114213
Supporting Variants
Samplessample157
Known GenesLMO4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083588
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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