A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625765



Internal ID6665913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27146261..27150584hg38UCSC Ensembl
Innerchr11:27146266..27150580hg38UCSC Ensembl
Outerchr11:27146257..27150589hg38UCSC Ensembl
chr11:27167808..27172131hg19UCSC Ensembl
Innerchr11:27167813..27172127hg19UCSC Ensembl
Outerchr11:27167804..27172136hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg384324
hg194324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14071733, essv14071732
SamplesHG03547, HG02642
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625765
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer