A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6857279



Internal ID10255034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:93554450..93554599hg38UCSC Ensembl
Outerchr12:93948226..93948375hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746222, esv2746220, esv2746221, esv2746218
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)essv6857279
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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