A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2973969



Internal ID15431089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:110695500..110698324hg38UCSC Ensembl
InnerchrX:109938728..109941552hg19UCSC Ensembl
InnerchrX:109825384..109828208hg18UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg382825
hg192825
hg182825
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515161
Supporting Variants
SamplesNA21313
Known GenesCHRDL1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2973969
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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