A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512400



Internal ID15851825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68133590..68136885hg38UCSC Ensembl
Outerchr15:68425928..68429223hg19UCSC Ensembl
Outerchr15:66212982..66216277hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383296
hg193296
hg183296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624990
Samples1
Known GenesPIAS1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512400
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