A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243498



Internal ID21307838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137154526..137172260hg38UCSC Ensembl
Outerchr4:137146964..137173804hg38UCSC Ensembl
Innerchr4:138075680..138093414hg19UCSC Ensembl
Outerchr4:138068118..138094958hg19UCSC Ensembl
Innerchr4:138295130..138312864hg18UCSC Ensembl
Outerchr4:138287568..138314408hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3826841
hg1926841
hg1826841
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169804
Supporting Variants
SamplesNGO_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243498
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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