A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511296



Internal ID15850721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1663734..1664149hg38UCSC Ensembl
Outerchr5:1661282..1670254hg38UCSC Ensembl
Innerchr5:1663849..1664264hg19UCSC Ensembl
Outerchr5:1661397..1670369hg19UCSC Ensembl
Innerchr5:1716849..1717264hg18UCSC Ensembl
Outerchr5:1714397..1723369hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg388973
hg198973
hg188973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625188
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)nsv511296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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