A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv324e201



Internal ID22759682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3469031..3469897hg38UCSC Ensembl
chr16:3519031..3519897hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2750406, esv2750404, esv2750402
SamplesSSM100, SSM071, SSM075, SSM065, SSM087, SSM097, SSM039, SSM073, SSM093, SSM088, SSM023, SSM058, SSM092, SSM084, SSM061, SSM029, SSM026, SSM019, SSM032, SSM003, SSM006, SSM040, SSM072, SSM020, SSM007, SSM078, SSM016, SSM077, SSM043, SSM049, SSM030
Known GenesNAA60
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)dgv324e201
Frequency
Sample Size96
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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