A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2746532



Internal ID9980816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:124373031..124373639hg38UCSC Ensembl
Outerchr12:124857577..124858185hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6959386, essv6842508, essv6809444, essv6746915, essv6879551, essv6823701, essv6779534, essv6783629, essv6894718, essv6965898, essv6791919, essv6819795, essv6827786, essv6953298, essv6673262, essv6677900, essv6857326
SamplesSSM027, SSM055, SSM084, SSM078, SSM031, SSM025, SSM032, SSM067, SSM093, SSM087, SSM079, SSM068, SSM075, SSM026, SSM098, SSM070, SSM080
Known GenesNCOR2
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)esv2746532
Frequency
Sample Size96
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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