A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5669237



Internal ID9250603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2257589..2259198hg38UCSC Ensembl
Outerchr19:2257552..2259248hg38UCSC Ensembl
Innerchr19:2257588..2259197hg19UCSC Ensembl
Outerchr19:2257551..2259247hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668914
Supporting Variants
SamplesNA12058
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5669237
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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