A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16075214



Internal ID6077097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49461676..49475440hg38UCSC Ensembl
chr19:49964933..49978697hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3813765
hg1913765
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644624
Supporting Variants
SamplesHG02395
Known GenesALDH16A1, FLT3LG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16075214
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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