A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511263



Internal ID15850688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38263010..38263650hg38UCSC Ensembl
Outerchr4:38262272..38268745hg38UCSC Ensembl
Innerchr4:38264631..38265271hg19UCSC Ensembl
Outerchr4:38263893..38270366hg19UCSC Ensembl
Innerchr4:37941026..37941666hg18UCSC Ensembl
Outerchr4:37940288..37946761hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386474
hg196474
hg186474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624822
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)nsv511263
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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