A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6929662



Internal ID9641190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149981434..149981652hg38UCSC Ensembl
Outerchr6:150302570..150302788hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732871, esv2732866, esv2732870
Supporting Variants
SamplesSSM003
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)essv6929662
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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