A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6962888



Internal ID9721998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68925096..68925448hg38UCSC Ensembl
Outerchr4:69790814..69791166hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727776, esv2727775
Supporting Variants
SamplesSSM027
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)essv6962888
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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