A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6923141



Internal ID9685697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:107073071..107073414hg38UCSC Ensembl
Outerchr6:107394275..107394618hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732546, esv2732547
Supporting Variants
SamplesSSM018
Known GenesBEND3
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)essv6923141
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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