A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640463



Internal ID6680550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36087997..36096019hg38UCSC Ensembl
chr17:34415343..34423413hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388023
hg198071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15665349, essv15665348, essv15665350
SamplesNA19323, HG02373, HG02060
Known GenesCCL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640463
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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