A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625942



Internal ID7012776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35967077..35968617hg38UCSC Ensembl
Innerchr11:35967127..35968567hg38UCSC Ensembl
Outerchr11:35967027..35968667hg38UCSC Ensembl
chr11:35988627..35990167hg19UCSC Ensembl
Innerchr11:35988677..35990117hg19UCSC Ensembl
Outerchr11:35988577..35990217hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090455
SamplesHG00598
Known GenesLDLRAD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625942
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