A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6702096



Internal ID9766671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28901708..28901853hg38UCSC Ensembl
Outerchr10:29190637..29190782hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734606, esv2734872
Supporting Variants
SamplesSSM039
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)essv6702096
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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