A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15063



Internal ID15827912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149568324..149568782hg38UCSC Ensembl
Outerchr6:149567837..149569974hg38UCSC Ensembl
Innerchr6:149889460..149889918hg19UCSC Ensembl
Innerchr6:149931153..149931611hg18UCSC Ensembl
Outerchr6:149930666..149932803hg18UCSC Ensembl
Innerchr6:150065072..150065530hg17UCSC Ensembl
Outerchr6:150064585..150066722hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382138
hg19459
hg182138
hg172138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7977
Supporting Variants
SamplesNA07048
Known GenesGINM1
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv15063
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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