A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511436



Internal ID15850861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4666435..4668106hg38UCSC Ensembl
Outerchr10:4658776..4669572hg38UCSC Ensembl
Innerchr10:4708627..4710298hg19UCSC Ensembl
Outerchr10:4700968..4711764hg19UCSC Ensembl
Innerchr10:4698627..4700298hg18UCSC Ensembl
Outerchr10:4690968..4701764hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810797
hg1910797
hg1810797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626048
Samples1
Known GenesLINC00704, LINC00705
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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