A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6880213



Internal ID9928990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21776869..21777073hg38UCSC Ensembl
Outerchr19:21959671..21959875hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718335, esv2718343, esv2718345, esv2718337, esv2718342
Supporting Variants
SamplesSSM093
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)essv6880213
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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