A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523448



Internal ID18821729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48736393..48772269hg38UCSC Ensembl
Innerchr13:49310529..49346405hg19UCSC Ensembl
Innerchr13:48208530..48244406hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3835877
hg1935877
hg1835877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036621
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)nssv3523448
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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