A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738696



Internal ID10322332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79506811..79507335hg38UCSC Ensembl
Outerchr10:81266567..81267091hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6769287
SamplesSSM008
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)esv2738696
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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