A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611513



Internal ID6651731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162304870..162420402hg38UCSC Ensembl
Innerchr6:162305370..162419902hg38UCSC Ensembl
Outerchr6:162303870..162421402hg38UCSC Ensembl
chr6:162725902..162841434hg19UCSC Ensembl
Innerchr6:162726402..162840934hg19UCSC Ensembl
Outerchr6:162724902..162842434hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38115533
hg19115533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621114, essv12621115, essv12621117, essv12621113, essv12621116
SamplesHG01051, NA19076, HG01323, HG03084, HG00593
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611513
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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