A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002806



Internal ID18745338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192227337..192251936hg38UCSC Ensembl
Innerchr3:191945126..191969725hg19UCSC Ensembl
Innerchr3:193427820..193452419hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3824600
hg1924600
hg1824600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611352
Samples
Known GenesFGF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002806
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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