A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2726908



Internal ID5037640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:3524369..3524561hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6910763, essv6836863, essv6697506, essv6962728, essv6889634, essv6683438, essv6693571, essv6951325, essv6810846, essv6722701, essv6926306, essv6929852, essv6730323
SamplesSSM027, SSM025, SSM020, SSM045, SSM083, SSM097, SSM047, SSM037, SSM034, SSM038, SSM019, SSM015, SSM076
Known GenesLRPAP1
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2726908
Frequency
Sample Size96
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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