A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608389



Internal ID6648628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25695293..25711977hg38UCSC Ensembl
chr6:25695521..25712205hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3816685
hg1916685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232478
SamplesNA19041
Known GenesSCGN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608389
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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