A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523413



Internal ID15450706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156878258..156911955hg38UCSC Ensembl
Innerchr6:157199392..157233089hg19UCSC Ensembl
Innerchr6:157241084..157274781hg18UCSC Ensembl
Innerchr6:157291505..157325202hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3833698
hg1933698
hg1833698
hg1733698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699164
Samples
Known GenesARID1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523413
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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