A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009804



Internal ID19099023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85472834..85532236hg38UCSC Ensembl
Innerchr3:85521984..85581386hg19UCSC Ensembl
Innerchr3:85604674..85664076hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3859403
hg1959403
hg1859403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596271
Samples
Known GenesCADM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009804
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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