A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511404



Internal ID15850829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40917225..40921819hg38UCSC Ensembl
Outerchr8:40915989..40924039hg38UCSC Ensembl
Innerchr8:40774744..40779338hg19UCSC Ensembl
Outerchr8:40773508..40781558hg19UCSC Ensembl
Innerchr8:40893901..40898495hg18UCSC Ensembl
Outerchr8:40892665..40900715hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388051
hg198051
hg188051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626012
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)nsv511404
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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