A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525563



Internal ID15452856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:28991427..29025028hg38UCSC Ensembl
Innerchr2:29214293..29247894hg19UCSC Ensembl
Innerchr2:29067797..29101398hg18UCSC Ensembl
Innerchr2:29125944..29159545hg17UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3833602
hg1933602
hg1833602
hg1733602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv213n21
Supporting Variantsnssv701702
Samples
Known GenesFAM179A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525563
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