A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2994384



Internal ID15667121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:9398382..9424967hg38UCSC Ensembl
InnerchrX:9366422..9393007hg19UCSC Ensembl
InnerchrX:9326422..9353007hg18UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3826586
hg1926586
hg1826586
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515222
Supporting Variants
SamplesNA18506
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2994384
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