A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5931314



Internal ID9660443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16547843..16549311hg38UCSC Ensembl
Outerchr19:16547686..16549498hg38UCSC Ensembl
Innerchr19:16658654..16660122hg19UCSC Ensembl
Outerchr19:16658497..16660309hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381813
hg191813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675983
Supporting Variants
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5931314
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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