A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525574



Internal ID18823855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107514878..107534615hg38UCSC Ensembl
Innerchr13:108167226..108186963hg19UCSC Ensembl
Innerchr13:106965227..106984964hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3819738
hg1919738
hg1819738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046112
Supporting Variants
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)nssv3525574
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