A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv387e201



Internal ID20125274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732675..89733035hg38UCSC Ensembl
chr16:89799083..89799443hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2715201, esv2715200
SamplesSSM086, SSM088, SSM089, SSM031, SSM035, SSM087, SSM038, SSM075, SSM026
Known GenesZNF276
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)dgv387e201
Frequency
Sample Size96
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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