A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16063071



Internal ID6357117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43383591..43418114hg38UCSC Ensembl
chr19:43887743..43922266hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3834524
hg1934524
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644466
Supporting Variants
SamplesNA20287
Known GenesTEX101
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16063071
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer