A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6212949



Internal ID9611990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27759411..27762823hg38UCSC Ensembl
chr19:28250319..28253731hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg383413
hg193413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675936
Supporting Variants
SamplesNA19313
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6212949
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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