A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5402635



Internal ID9302955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46027425..46030318hg38UCSC Ensembl
Outerchr19:46027268..46030471hg38UCSC Ensembl
Innerchr19:46530683..46533576hg19UCSC Ensembl
Outerchr19:46530526..46533729hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383204
hg193204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659252
Supporting Variants
SamplesNA18486
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5402635
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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