A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734326



Internal ID9968653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:44836788..44838402hg38UCSC Ensembl
Outerchr7:44876387..44878001hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6935020
SamplesSSM021
Known GenesH2AFV
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)esv2734326
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