A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511268



Internal ID15850693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183753343..183754371hg38UCSC Ensembl
Outerchr4:183752115..183759753hg38UCSC Ensembl
Innerchr4:184674496..184675524hg19UCSC Ensembl
Outerchr4:184673268..184680906hg19UCSC Ensembl
Innerchr4:184911490..184912518hg18UCSC Ensembl
Outerchr4:184910262..184917900hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg387639
hg197639
hg187639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624877
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)nsv511268
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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