A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013774



Internal ID19102993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52989183..53005251hg38UCSC Ensembl
Innerchr3:53023199..53039267hg19UCSC Ensembl
Innerchr3:52998239..53014307hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3816069
hg1916069
hg1816069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4740n100
Supporting Variantsnssv3739881, nssv3595299
Samples
Known GenesSFMBT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013774
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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