A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6919872



Internal ID10030162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:95447290..95448014hg38UCSC Ensembl
Outerchr10:97207047..97207771hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739718
Supporting Variants
SamplesSSM017
Known GenesSORBS1
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)essv6919872
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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