A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6695584



Internal ID10109080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:78803735..78803854hg38UCSC Ensembl
Outerchr12:79197515..79197634hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746103, esv2746104, esv2746105
Supporting Variants
SamplesSSM037
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)essv6695584
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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