A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247635



Internal ID21306469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137168393..137173967hg38UCSC Ensembl
Outerchr4:137163953..137187209hg38UCSC Ensembl
Innerchr4:138089547..138095121hg19UCSC Ensembl
Outerchr4:138085107..138108363hg19UCSC Ensembl
Innerchr4:138308997..138314571hg18UCSC Ensembl
Outerchr4:138304557..138327813hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3823257
hg1923257
hg1823257
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169804
Supporting Variants
SamplesNGO_28
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247635
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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