A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644217



Internal ID7030973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34793329..34806277hg38UCSC Ensembl
chr19:35284233..35297181hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812949
hg1912949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16044801, essv16044808, essv16044809, essv16044802, essv16044804, essv16044807, essv16044806, essv16044805, essv16044803
SamplesHG01795, HG00671, HG02026, HG02356, HG02023, HG01849, HG02141, HG02355, HG02020
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644217
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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