A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6889032



Internal ID9666609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160660191..160661148hg38UCSC Ensembl
Outerchr6:161081223..161082180hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733056, esv2733055
Supporting Variants
SamplesSSM012
Known GenesLPA
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)essv6889032
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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