A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089356



Internal ID21268030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48925853..49090007hg38UCSC Ensembl
Innerchr4:48927870..49092024hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38164155
hg19164155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118225
Supporting Variants
Samplessample119
Known GenesCWH43
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089356
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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