A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6230262



Internal ID9207665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162144982..162226673hg38UCSC Ensembl
Outerchr6:162144945..162226723hg38UCSC Ensembl
Innerchr6:162566014..162647705hg19UCSC Ensembl
Outerchr6:162565977..162647755hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3881779
hg1981779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661302
Supporting Variants
SamplesNA19059
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6230262
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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