A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6918702



Internal ID9682424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29871285..29915244hg38UCSC Ensembl
Outerchr6:29839062..29883021hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843960
hg1943960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731769, esv2731767, esv2731775
Supporting Variants
SamplesSSM017
Known GenesHLA-H
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)essv6918702
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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