A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739875



Internal ID19038156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52988839..53004874hg38UCSC Ensembl
Innerchr3:53022855..53038890hg19UCSC Ensembl
Innerchr3:52997895..53013930hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3816036
hg1916036
hg1816036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003254
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)nssv3739875
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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