A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6838717



Internal ID9891829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132149083..132150671hg38UCSC Ensembl
Outerchr12:132633628..132635216hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381589
hg191589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746916
Supporting Variants
SamplesSSM083
Known GenesNOC4L
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)essv6838717
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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