A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529283



Internal ID18827564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68932575..69016461hg38UCSC Ensembl
Innerchr13:69506707..69590593hg19UCSC Ensembl
Innerchr13:68404708..68488594hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3883887
hg1983887
hg1883887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044793
Supporting Variants
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529283
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