A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6842093



Internal ID9894679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3061242..3061376hg38UCSC Ensembl
Outerchr10:3103434..3103568hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731106, esv2730995, esv2731095
Supporting Variants
SamplesSSM084
Known Genes
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)essv6842093
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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