A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963289



Internal ID16257245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52999279..53004770hg38UCSC Ensembl
Innerchr3:53033295..53038786hg19UCSC Ensembl
Innerchr3:53008335..53013826hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg385492
hg195492
hg185492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590337
Supporting Variants
Samples
Known GenesSFMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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