A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593106



Internal ID16033829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196969266..197002993hg38UCSC Ensembl
Innerchr3:196696137..196729864hg19UCSC Ensembl
Innerchr3:198180534..198214261hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3833728
hg1933728
hg1833728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987025
Samples
Known GenesMFI2, MFI2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593106
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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