A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2735350



Internal ID9969680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35150749..35151182hg38UCSC Ensembl
Outerchr10:35439677..35440110hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv96e201
Supporting Variantsessv6904617, essv6709233, essv6827374, essv6771761, essv6919824, essv6897414, essv6712722, essv6681289, essv6842134, essv6944551, essv6787427, essv6702104, essv6968707
SamplesSSM065, SSM039, SSM013, SSM042, SSM041, SSM023, SSM084, SSM069, SSM017, SSM033, SSM080, SSM004, SSM099
Known GenesCREM
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)esv2735350
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