A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611307



Internal ID6998216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153812617..153866253hg38UCSC Ensembl
chr6:154133752..154187388hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3853637
hg1953637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12592321
SamplesNA19308
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611307
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