A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2979384



Internal ID15664398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126920096..127116368hg38UCSC Ensembl
InnerchrX:126054079..126250351hg19UCSC Ensembl
InnerchrX:125881760..126078032hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38196273
hg19196273
hg18196273
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515169
Supporting Variants
SamplesNA18498
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2979384
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