A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525920



Internal ID15106527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:49891278..49911166hg38UCSC Ensembl
Innerchr12:50285061..50304949hg19UCSC Ensembl
Innerchr12:48571328..48591216hg18UCSC Ensembl
Innerchr12:48571328..48591216hg17UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3819889
hg1919889
hg1819889
hg1719889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702124
Samples
Known GenesFAIM2, LOC283332
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525920
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