A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661906



Internal ID4706240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162758927..162761143hg19UCSC Ensembl
Outerchr6:162758770..162761296hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv5903857, essv6071183, essv6025392
SamplesNA18535, HG00475, HG00542
Known GenesPARK2
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661906
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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