A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013733



Internal ID19102952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52988921..53005189hg38UCSC Ensembl
Innerchr3:53022937..53039205hg19UCSC Ensembl
Innerchr3:52997977..53014245hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3816269
hg1916269
hg1816269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4740n100
Supporting Variantsnssv3595292
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)nsv1013733
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