A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5480197



Internal ID8457600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6266526..6267171hg38UCSC Ensembl
chr19:6266537..6267182hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662795
Supporting Variants
SamplesNA18612
Known GenesMLLT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5480197
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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