A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6766692



Internal ID9829127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:236713462..236714017hg38UCSC Ensembl
Outerchr1:236876762..236877317hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725496
Supporting Variants
SamplesSSM064
Known GenesACTN2
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)essv6766692
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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