A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6902198



Internal ID10011593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6709859..6710481hg38UCSC Ensembl
Outerchr19:6709870..6710492hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718069
Supporting Variants
SamplesSSM012
Known GenesC3
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)essv6902198
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