A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2741873



Internal ID10295989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119519072..119521054hg38UCSC Ensembl
Outerchr10:121278584..121280566hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381983
hg191983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6976692, essv6827444, essv6709294, essv6720439
SamplesSSM041, SSM029, SSM044, SSM080
Known GenesRGS10
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)esv2741873
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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