A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6826898



Internal ID9661106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149981459..149981683hg38UCSC Ensembl
Outerchr6:150302595..150302819hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732871, esv2732866, esv2732870
Supporting Variants
SamplesSSM010
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)essv6826898
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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