A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14009007



Internal ID1862283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6123720..6150612hg38UCSC Ensembl
Innerchr11:6123720..6150612hg38UCSC Ensembl
Outerchr11:6123220..6151112hg38UCSC Ensembl
chr11:6144950..6171842hg19UCSC Ensembl
Innerchr11:6144950..6171842hg19UCSC Ensembl
Outerchr11:6144450..6172342hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826893
hg1926893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625260
Supporting Variants
SamplesHG01762
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14009007
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