A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6695191



Internal ID10108560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26574138..26627788hg38UCSC Ensembl
Outerchr10:26863067..26916717hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853651
hg1953651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734384
Supporting Variants
SamplesSSM037
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)essv6695191
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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