A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26226



Internal ID15491275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53609494..53790126hg38UCSC Ensembl
Outerchr15:53528808..53840415hg38UCSC Ensembl
Innerchr15:53901691..54082323hg19UCSC Ensembl
Outerchr15:53821005..54132612hg19UCSC Ensembl
Innerchr15:51688983..51869615hg18UCSC Ensembl
Outerchr15:51608297..51919904hg18UCSC Ensembl
Innerchr15:51688983..51869615hg17UCSC Ensembl
Outerchr15:51608297..51919904hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38311608
hg19311608
hg18311608
hg17311608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9267
Supporting Variants
SamplesNA18860
Known GenesWDR72
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)nssv26226
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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