A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611542



Internal ID6651760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162503572..162525380hg38UCSC Ensembl
chr6:162924604..162946412hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3821809
hg1921809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12621463, essv12621462, essv12621465, essv12621464
SamplesHG01051, HG01323, HG02182, HG00593
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611542
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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