A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5631293



Internal ID8608696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2898984..2904641hg38UCSC Ensembl
Outerchr19:2898947..2904691hg38UCSC Ensembl
Innerchr19:2898982..2904639hg19UCSC Ensembl
Outerchr19:2898945..2904689hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385745
hg195745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674415
Supporting Variants
SamplesNA19000
Known GenesZNF57
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5631293
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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