A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6775407



Internal ID10181348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26572853..26626553hg38UCSC Ensembl
Outerchr10:26861782..26915482hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853701
hg1953701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734384
Supporting Variants
SamplesSSM066
Known GenesLINC00264
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)essv6775407
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