A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6750374



Internal ID9811422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21567948..21568981hg38UCSC Ensembl
Outerchr19:21750750..21751783hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718335, esv2718325, esv2718338, esv2718337
Supporting Variants
SamplesSSM056
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)essv6750374
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer