A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611476



Internal ID6651694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161814032..161848545hg38UCSC Ensembl
chr6:162235064..162269577hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3834514
hg1934514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12619502
SamplesHG00280
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611476
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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