A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2718894



Internal ID9953186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:55203948..55204295hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv532e201
Supporting Variantsessv6824716, essv6946195, essv6674864, essv6961081, essv6971993, essv6868472, essv6678907, essv6797174, essv6804250, essv6967555, essv6820943, essv6703601, essv6685951, essv6852867, essv6863677
SamplesSSM071, SSM027, SSM079, SSM039, SSM073, SSM088, SSM023, SSM028, SSM026, SSM089, SSM032, SSM031, SSM086, SSM078, SSM034
Known Genes
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)esv2718894
Frequency
Sample Size96
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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