A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987026



Internal ID16280982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197002210..197003253hg38UCSC Ensembl
Innerchr3:196729081..196730124hg19UCSC Ensembl
Innerchr3:198213478..198214521hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381044
hg191044
hg181044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593107
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)nssv987026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer