A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317586



Internal ID4319402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132280887..132292976hg38UCSC Ensembl
chr11:132150781..132162870hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3812090
hg1912090
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628121
Supporting Variants
SamplesNA20795
Known GenesNTM, NTM-IT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317586
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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