A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6852076



Internal ID9661943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:143843239..143964336hg38UCSC Ensembl
Outerchr4:144764392..144885489hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38121098
hg19121098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2728476, esv2728477
Supporting Variants
SamplesSSM011
Known GenesGYPE
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)essv6852076
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