A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2746937



Internal ID9981221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132281947..132282272hg38UCSC Ensembl
Outerchr12:132858533..132858858hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6688369, essv6685175
SamplesSSM035, SSM034
Known GenesGALNT9
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)esv2746937
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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