A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv963e201



Internal ID20125850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177467804..177468231hg38UCSC Ensembl
chr5:176894805..176895232hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2731194, esv2731197
SamplesSSM027, SSM024, SSM045, SSM065, SSM087, SSM039, SSM041, SSM084, SSM047, SSM018, SSM017, SSM031, SSM086, SSM081, SSM072, SSM020, SSM022, SSM025
Known GenesDBN1
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv963e201
Frequency
Sample Size96
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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