A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248805



Internal ID21311947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137171041..137173967hg38UCSC Ensembl
Outerchr4:137170949..137187209hg38UCSC Ensembl
Innerchr4:138092195..138095121hg19UCSC Ensembl
Outerchr4:138092103..138108363hg19UCSC Ensembl
Innerchr4:138311645..138314571hg18UCSC Ensembl
Outerchr4:138311553..138327813hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3816261
hg1916261
hg1816261
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169804
Supporting Variants
SamplesSNI_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248805
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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