A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739880



Internal ID19038161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52988921..53004916hg38UCSC Ensembl
Innerchr3:53022937..53038932hg19UCSC Ensembl
Innerchr3:52997977..53013972hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3815996
hg1915996
hg1815996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013928
Supporting Variants
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)nssv3739880
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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