A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2746435



Internal ID5057167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:117759639..117759987hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6924416, essv6953293, essv6815526, essv6940414
SamplesSSM022, SSM025, SSM077, SSM018
Known GenesNOS1
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2746435
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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