A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15969608



Internal ID4919328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2733028..2744541hg38UCSC Ensembl
chr19:2733026..2744539hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811514
hg1911514
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643437
Supporting Variants
SamplesNA12760
Known GenesSLC39A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15969608
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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