A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511457



Internal ID15504196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496273..76498584hg38UCSC Ensembl
Outerchr10:76486334..76500936hg38UCSC Ensembl
Innerchr10:78256031..78258342hg19UCSC Ensembl
Outerchr10:78246092..78260694hg19UCSC Ensembl
Innerchr10:77926037..77928348hg18UCSC Ensembl
Outerchr10:77916098..77930700hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3814603
hg1914603
hg1814603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626071
Samples1
Known GenesC10orf11
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511457
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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