A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6841361



Internal ID9894022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149984196..149984503hg38UCSC Ensembl
Outerchr6:150305332..150305639hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732877, esv2732866, esv2732872
Supporting Variants
SamplesSSM084
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)essv6841361
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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