A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644065



Internal ID6684133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27348171..28149207hg38UCSC Ensembl
chr19:27839079..28640114hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38801037
hg19801036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16027788, essv16027789, essv16027790
SamplesHG03900, HG02450, HG02881
Known GenesLINC00662
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644065
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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