A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5783066



Internal ID9716018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41186238..41191773hg38UCSC Ensembl
chr19:41692143..41697678hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385536
hg195536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669501
Supporting Variants
SamplesNA19468
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5783066
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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