A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750337



Internal ID10331307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1397101..1397428hg38UCSC Ensembl
Outerchr16:1447102..1447429hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv322e201
Supporting Variantsessv6911597, essv6835312, essv6953746, essv6932352
SamplesSSM002, SSM082, SSM020, SSM025
Known GenesUNKL
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)esv2750337
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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