A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6890066



Internal ID9666516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56694291..56702231hg38UCSC Ensembl
Outerchr7:56761984..56769924hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg387941
hg197941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734469, esv2734448, esv2734468
Supporting Variants
SamplesSSM012
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)essv6890066
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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