A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6974702



Internal ID9736552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29978807..29980646hg38UCSC Ensembl
Outerchr6:29946584..29948423hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731778, esv2731779, esv2731776, esv2731777
Supporting Variants
SamplesSSM029
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)essv6974702
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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