A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529304



Internal ID18827585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70198751hg38UCSC Ensembl
Innerchr13:70736064..70772883hg19UCSC Ensembl
Innerchr13:69634065..69670884hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3836820
hg1936820
hg1836820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046521
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529304
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