A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090665



Internal ID21272507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92956228..93066135hg38UCSC Ensembl
Innerchr4:93877379..93987286hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38109908
hg19109908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118232
Supporting Variants
Samplessample178
Known GenesGRID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090665
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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