A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625977



Internal ID7012811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37330791..37363594hg38UCSC Ensembl
Innerchr11:37330791..37363594hg38UCSC Ensembl
Outerchr11:37330291..37364094hg38UCSC Ensembl
chr11:37352341..37385144hg19UCSC Ensembl
Innerchr11:37352341..37385144hg19UCSC Ensembl
Outerchr11:37351841..37385644hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3832804
hg1932804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14092100
SamplesHG02852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625977
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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