A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987031



Internal ID16280987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197002210..197003311hg38UCSC Ensembl
Innerchr3:196729081..196730182hg19UCSC Ensembl
Innerchr3:198213478..198214579hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381102
hg191102
hg181102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593108
Supporting Variants
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)nssv987031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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