A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674415



Internal ID9593834
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5631293, essv6400882
SamplesNA18977, NA19000
Known GenesZNF57
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674415
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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