A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6775660



Internal ID10181576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:2768205..2768679hg38UCSC Ensembl
Outerchr12:2877371..2877845hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745421, esv2745420
Supporting Variants
SamplesSSM066
Known GenesLOC283440
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)essv6775660
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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