A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014365



Internal ID18756899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141516537..141563773hg38UCSC Ensembl
Innerchr3:141235379..141282615hg19UCSC Ensembl
Innerchr3:142718069..142765305hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3847237
hg1947237
hg1847237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606102
Samples
Known GenesRASA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014365
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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