A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523778



Internal ID15451071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51180971..51194365hg38UCSC Ensembl
Innerchr13:51755107..51768501hg19UCSC Ensembl
Innerchr13:50653108..50666502hg18UCSC Ensembl
Innerchr13:50653108..50666502hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3813395
hg1913395
hg1813395
hg1713395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699601
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523778
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