A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763181



Internal ID10169483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26572851..26626647hg38UCSC Ensembl
Outerchr10:26861780..26915576hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853797
hg1953797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734384
Supporting Variants
SamplesSSM062
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)essv6763181
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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