A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511582



Internal ID15851007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28453543..28455297hg38UCSC Ensembl
Outerchr17:28448723..28461026hg38UCSC Ensembl
Innerchr17:26780561..26782315hg19UCSC Ensembl
Outerchr17:26775741..26788044hg19UCSC Ensembl
Innerchr17:23804688..23806442hg18UCSC Ensembl
Outerchr17:23799868..23812171hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3812304
hg1912304
hg1812304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626209
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)nsv511582
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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