A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6866686



Internal ID10263499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5648262..5648496hg38UCSC Ensembl
Outerchr10:5690225..5690459hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731818
Supporting Variants
SamplesSSM089
Known GenesASB13
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)essv6866686
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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