A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251815



Internal ID21303207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137171041..137172260hg38UCSC Ensembl
Outerchr4:137170949..137173804hg38UCSC Ensembl
Innerchr4:138092195..138093414hg19UCSC Ensembl
Outerchr4:138092103..138094958hg19UCSC Ensembl
Innerchr4:138311645..138312864hg18UCSC Ensembl
Outerchr4:138311553..138314408hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg382856
hg192856
hg182856
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169804
Supporting Variants
SamplesMLY_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251815
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer