A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008370



Internal ID19097588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59292472..59394285hg38UCSC Ensembl
Innerchr3:59278198..59380011hg19UCSC Ensembl
Innerchr3:59253238..59355051hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38101814
hg19101814
hg18101814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593394
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)nsv1008370
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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