A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739596



Internal ID10323232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:92400045..92409624hg38UCSC Ensembl
Outerchr10:94159802..94169381hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389580
hg199580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6803290, essv6743827
SamplesSSM073, SSM053
Known Genes
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)esv2739596
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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