A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21524



Internal ID15834321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138231184..138233285hg38UCSC Ensembl
Outerchr9:138231167..138233418hg38UCSC Ensembl
Innerchr9:141121634..141123735hg19UCSC Ensembl
Outerchr9:141121617..141123868hg19UCSC Ensembl
Innerchr9:140241455..140243556hg18UCSC Ensembl
Outerchr9:140241438..140243689hg18UCSC Ensembl
Innerchr9:138397471..138399572hg17UCSC Ensembl
Outerchr9:138397454..138399705hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382252
hg192252
hg182252
hg172252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8590
Supporting Variants
SamplesNA18517
Known GenesFAM157B
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)nssv21524
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