A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609933



Internal ID6996852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91122338..91135696hg38UCSC Ensembl
chr6:91832056..91845414hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3813359
hg1913359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12461656
SamplesNA19394
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609933
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