A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963319



Internal ID16257275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53043356..53045872hg38UCSC Ensembl
Innerchr3:53077372..53079888hg19UCSC Ensembl
Innerchr3:53052412..53054928hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg382517
hg192517
hg182517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590342
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)nssv963319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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