A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092164



Internal ID21275444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163689594..163693731hg38UCSC Ensembl
Innerchr4:164610746..164614883hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg384138
hg194138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113562
Supporting Variants
Samplessample222
Known GenesMARCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092164
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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