A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608444



Internal ID6995373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27846413..27862239hg38UCSC Ensembl
chr6:27814191..27830017hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3815827
hg1915827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12238830, essv12238829, essv12238831, essv12238832
SamplesHG00338, HG02180, HG01113, HG02052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608444
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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