A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6678938



Internal ID9745781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:57499415..57499636hg38UCSC Ensembl
Outerchr19:58010783..58011004hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2719071, esv2719074, esv2719079, esv2719076, esv2719072, esv2719078
Supporting Variants
SamplesSSM032
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)essv6678938
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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