A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526811



Internal ID15107418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67480195..67482357hg38UCSC Ensembl
Innerchr14:67946912..67949074hg19UCSC Ensembl
Innerchr14:67016665..67018827hg18UCSC Ensembl
Innerchr14:67016665..67018827hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382163
hg192163
hg182163
hg172163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703165
Samples
Known GenesTMEM229B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526811
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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