A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626083



Internal ID15849616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28985728..28990098hg38UCSC Ensembl
Outerchr11:28980690..28991074hg38UCSC Ensembl
Innerchr11:29007275..29011645hg19UCSC Ensembl
Outerchr11:29002237..29012621hg19UCSC Ensembl
Innerchr11:28963851..28968221hg18UCSC Ensembl
Outerchr11:28958813..28969197hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3810385
hg1910385
hg1810385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511468
Supporting Variants
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)nssv626083
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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