A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115430



Internal ID21298696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48711167..48715835hg38UCSC Ensembl
InnerchrX:48569558..48574240hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg384669
hg194683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1265n145
Supporting Variantsnssv14101722
Samplessample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115430
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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