A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593361



Internal ID18891642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52994359..53011897hg38UCSC Ensembl
Innerchr3:53028375..53045913hg19UCSC Ensembl
Innerchr3:53003415..53020953hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3817539
hg1917539
hg1817539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997853
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)nssv3593361
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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