A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511599



Internal ID15851024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20439885..20454994hg38UCSC Ensembl
Outerchr17:20437212..20472713hg38UCSC Ensembl
Innerchr17:20343198..20358307hg19UCSC Ensembl
Outerchr17:20340525..20376026hg19UCSC Ensembl
Innerchr17:20283790..20298899hg18UCSC Ensembl
Outerchr17:20281117..20316618hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3835502
hg1935502
hg1835502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626228
Samples1
Known GenesLGALS9B
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511599
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer