A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611554



Internal ID6651772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162562354..162659812hg38UCSC Ensembl
Innerchr6:162562369..162659798hg38UCSC Ensembl
Outerchr6:162562340..162659827hg38UCSC Ensembl
chr6:162983386..163080844hg19UCSC Ensembl
Innerchr6:162983401..163080830hg19UCSC Ensembl
Outerchr6:162983372..163080859hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3897459
hg1997459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1237e214
Supporting Variantsessv12621508, essv12621507
SamplesHG02272, HG01620
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611554
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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