A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6923998



Internal ID10033337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44414365..44414925hg38UCSC Ensembl
Outerchr10:44909813..44910373hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735928
Supporting Variants
SamplesSSM018
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)essv6923998
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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