A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6697426



Internal ID10111904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126915778..126917237hg38UCSC Ensembl
Outerchr3:126634621..126636080hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725877
Supporting Variants
SamplesSSM038
Known GenesCHCHD6
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)essv6697426
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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