A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043834



Internal ID19133053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30837991..30861455hg38UCSC Ensembl
Innerchr13:31412128..31435592hg19UCSC Ensembl
Innerchr13:30310128..30333592hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3823465
hg1923465
hg1823465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1624n100
Supporting Variantsnssv3523225, nssv3523224
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)nsv1043834
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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