A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6755367



Internal ID10163142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131110968..131114504hg38UCSC Ensembl
Outerchr10:132909231..132912767hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383537
hg193537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743528
Supporting Variants
SamplesSSM058
Known GenesTCERG1L
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)essv6755367
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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