A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627880



Internal ID6668024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119000685..119001245hg38UCSC Ensembl
Innerchr11:119000706..119001224hg38UCSC Ensembl
Outerchr11:119000664..119001266hg38UCSC Ensembl
chr11:118871395..118871955hg19UCSC Ensembl
Innerchr11:118871416..118871934hg19UCSC Ensembl
Outerchr11:118871374..118871976hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293225, essv14293228, essv14293227, essv14293226, essv14293229
SamplesNA20877, HG04156, NA21119, NA21141, NA21093
Known GenesCCDC84
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627880
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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