A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511462



Internal ID15850887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:679001..679803hg38UCSC Ensembl
Outerchr10:673863..688289hg38UCSC Ensembl
Innerchr10:724941..725743hg19UCSC Ensembl
Outerchr10:719803..734229hg19UCSC Ensembl
Innerchr10:714941..715743hg18UCSC Ensembl
Outerchr10:709803..724229hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3814427
hg1914427
hg1814427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626076
Samples1
Known GenesDIP2C
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511462
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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