A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611475



Internal ID6651693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161814032..161848545hg38UCSC Ensembl
chr6:162235064..162269577hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3834514
hg1934514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1232e214
Supporting Variantsessv12619501
SamplesNA20754
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611475
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