A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014299



Internal ID19103520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6601130..6611633hg38UCSC Ensembl
Innerchr3:6642817..6653320hg19UCSC Ensembl
Innerchr3:6617817..6628320hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810504
hg1910504
hg1810504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4672n100
Supporting Variantsnssv3591822, nssv3739585, nssv3591821
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014299
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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