A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6855760



Internal ID10253667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:135797407..135797500hg38UCSC Ensembl
Outerchr7:135482155..135482248hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735192, esv2735193, esv2735194
Supporting Variants
SamplesSSM087
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)essv6855760
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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