A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715200



Internal ID9949486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89732675..89733035hg38UCSC Ensembl
Outerchr16:89799083..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 Variantsdgv387e201
Supporting Variantsessv6809852, essv6863110, essv6688790, essv6960313, essv6852161, essv6867914, essv6858148, essv6699161, essv6674168, essv6867913
SamplesSSM075, SSM087, SSM038, SSM088, SSM026, SSM089, SSM035, SSM031, SSM086
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)esv2715200
Frequency
Sample Size96
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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