A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611532



Internal ID6651750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162387755..162664564hg38UCSC Ensembl
Innerchr6:162387774..162664545hg38UCSC Ensembl
Outerchr6:162387736..162664583hg38UCSC Ensembl
chr6:162808787..163085596hg19UCSC Ensembl
Innerchr6:162808806..163085577hg19UCSC Ensembl
Outerchr6:162808768..163085615hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38276810
hg19276810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621277, essv12621276
SamplesHG02272, HG01051
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611532
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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