A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887204



Internal ID9935458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56149990..56152530hg38UCSC Ensembl
Outerchr7:56217683..56220223hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg382541
hg192541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734454, esv2734448, esv2734447
Supporting Variants
SamplesSSM096
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)essv6887204
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