A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626182



Internal ID15503029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72095726hg38UCSC Ensembl
Outerchr15:72093834..72115728hg38UCSC Ensembl
Innerchr15:72386349..72388067hg19UCSC Ensembl
Outerchr15:72386175..72408069hg19UCSC Ensembl
Innerchr15:70173403..70175121hg18UCSC Ensembl
Outerchr15:70173229..70195123hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3821895
hg1921895
hg1821895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511557
Supporting Variants
Samples1
Known GenesMYO9A, SENP8
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626182
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