A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511323



Internal ID15850748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17377704..17380546hg38UCSC Ensembl
Outerchr6:17376435..17380777hg38UCSC Ensembl
Innerchr6:17377935..17380777hg19UCSC Ensembl
Outerchr6:17376666..17381008hg19UCSC Ensembl
Innerchr6:17485914..17488756hg18UCSC Ensembl
Outerchr6:17484645..17488987hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384343
hg194343
hg184343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n50
Supporting Variantsnssv625489
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)nsv511323
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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