A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110656



Internal ID21293922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54529031..54532535hg38UCSC Ensembl
InnerchrX:54555464..54558968hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg383505
hg193505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266n145
Supporting Variantsnssv14101654, nssv14104968
Samplessample147, sample275
Known GenesGNL3L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110656
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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