A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511235



Internal ID15850660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43749671..43749983hg38UCSC Ensembl
Outerchr4:43749619..43759196hg38UCSC Ensembl
Innerchr4:43751688..43752000hg19UCSC Ensembl
Outerchr4:43751636..43761213hg19UCSC Ensembl
Innerchr4:43446445..43446757hg18UCSC Ensembl
Outerchr4:43446393..43455970hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg389578
hg199578
hg189578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624511
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511235
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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