A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611557



Internal ID6651775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162578005..162633015hg38UCSC Ensembl
chr6:162999037..163054047hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3855011
hg1955011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621513, essv12621515, essv12621514
SamplesHG02702, NA20787, NA18620
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611557
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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