A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16043761



Internal ID4926435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33718830..33745191hg38UCSC Ensembl
chr19:34209735..34236096hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3826362
hg1926362
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644193
Supporting Variants
SamplesNA12762
Known GenesCHST8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16043761
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