A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6910863



Internal ID9676685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:68925046..68925475hg38UCSC Ensembl
Outerchr4:69790764..69791193hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727776, esv2727775
Supporting Variants
SamplesSSM015
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)essv6910863
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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