A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6785476



Internal ID10003206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:120133364..120134106hg38UCSC Ensembl
Outerchr1:120675935..120676677hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716829
Supporting Variants
SamplesSSM009
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)essv6785476
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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