A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644649



Internal ID7031403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50730434..50740763hg38UCSC Ensembl
chr19:51233691..51244020hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3810330
hg1910330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16078594, essv16078595, essv16078593
SamplesHG01670, HG01597, NA20803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644649
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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