A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6776584



Internal ID9835720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:57190111..57190701hg38UCSC Ensembl
Outerchr20:55765167..55765757hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722598
Supporting Variants
SamplesSSM066
Known GenesBMP7
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)essv6776584
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