A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644081



Internal ID6684149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27755925..27983639hg38UCSC Ensembl
chr19:28246833..28474547hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38227715
hg19227715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv658e214
Supporting Variantsessv16031164, essv16031162, essv16031163
SamplesHG02450, HG03900, HG02881
Known GenesLINC00662
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644081
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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