A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624966



Internal ID15848502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26385071..26385435hg38UCSC Ensembl
Outerchr5:26383898..26393896hg38UCSC Ensembl
Innerchr5:26385180..26385544hg19UCSC Ensembl
Outerchr5:26384007..26394005hg19UCSC Ensembl
Innerchr5:26420937..26421301hg18UCSC Ensembl
Outerchr5:26419764..26429762hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg389999
hg199999
hg189999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511276
Supporting Variants
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)nssv624966
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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