A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6698550



Internal ID9764092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495772..76501266hg38UCSC Ensembl
Outerchr10:78255530..78261024hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385495
hg195495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738451
Supporting Variants
SamplesSSM038
Known GenesC10orf11
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)essv6698550
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