A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6943552



Internal ID9705429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:150013933..150037136hg38UCSC Ensembl
Outerchr6:150335069..150358272hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3823204
hg1923204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732879, esv2732878
Supporting Variants
SamplesSSM023
Known GenesRAET1L
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)essv6943552
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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