A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051067



Internal ID19140286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107514878..107528415hg38UCSC Ensembl
Innerchr13:108167226..108180763hg19UCSC Ensembl
Innerchr13:106965227..106978764hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3813538
hg1913538
hg1813538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525573
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051067
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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