A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6366928



Internal ID9611201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34849104..34851672hg38UCSC Ensembl
chr19:35340008..35342576hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382569
hg192569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658256
Supporting Variants
SamplesNA19312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6366928
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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