A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5400999



Internal ID8378402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053911..12066782hg38UCSC Ensembl
chr19:12164726..12177597hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812872
hg1912872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668294
Supporting Variants
SamplesNA18542
Known GenesZNF844
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5400999
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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