A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242579



Internal ID21308196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66514883..66527245hg38UCSC Ensembl
Outerchr4:66512370..66530383hg38UCSC Ensembl
Innerchr4:67380601..67392963hg19UCSC Ensembl
Outerchr4:67378088..67396101hg19UCSC Ensembl
Innerchr4:67063196..67075558hg18UCSC Ensembl
Outerchr4:67060683..67078696hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3818014
hg1918014
hg1818014
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169996
Supporting Variants
SamplesNGO_40
Known GenesMIR548AJ2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242579
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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