A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6758884



Internal ID9817827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:42951445..43042450hg38UCSC Ensembl
Outerchr19:43455597..43546602hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3891006
hg1991006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718594, esv2718602, esv2718601, esv2718599
Supporting Variants
SamplesSSM059
Known GenesPSG11
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)essv6758884
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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