A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113762



Internal ID21297028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31434684..31436544hg38UCSC Ensembl
InnerchrX:31452801..31454661hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1263n145
Supporting Variantsnssv14101862, nssv14101714, nssv14101688, nssv14101854
Samplessample425, sample313, sample420, sample302
Known GenesDMD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113762
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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