A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611533



Internal ID6651751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162422967..162470500hg38UCSC Ensembl
chr6:162843999..162891532hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3847534
hg1947534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621278, essv12621279, essv12621281, essv12621280
SamplesHG01051, HG00593, HG02182, HG01323
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611533
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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