A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6770696



Internal ID10177110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:4020698..4020988hg38UCSC Ensembl
Outerchr6:4020932..4021222hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731499
Supporting Variants
SamplesSSM065
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)essv6770696
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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