A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1237e214



Internal ID20122660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162562354..162674622hg38UCSC Ensembl
chr6:162983386..163095654hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38112269
hg19112269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611558, esv3611554
SamplesHG02272, HG01620
Known GenesPARK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1237e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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