A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249326



Internal ID21310780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121360818..121363980hg38UCSC Ensembl
Outerchr4:121353499..121369976hg38UCSC Ensembl
Innerchr4:122281973..122285135hg19UCSC Ensembl
Outerchr4:122274654..122291131hg19UCSC Ensembl
Innerchr4:122501423..122504585hg18UCSC Ensembl
Outerchr4:122494104..122510581hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3816478
hg1916478
hg1816478
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170082
Supporting Variants
SamplesPML_1
Known GenesQRFPR
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249326
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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