A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511559



Internal ID15850984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53907812..53910302hg38UCSC Ensembl
Outerchr15:53905130..53912067hg38UCSC Ensembl
Innerchr15:54200009..54202499hg19UCSC Ensembl
Outerchr15:54197327..54204264hg19UCSC Ensembl
Innerchr15:51987301..51989791hg18UCSC Ensembl
Outerchr15:51984619..51991556hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg386938
hg196938
hg186938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626184
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)nsv511559
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