A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5820083



Internal ID9489600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19428075..19429358hg38UCSC Ensembl
Outerchr17:19428038..19429408hg38UCSC Ensembl
Innerchr17:19331388..19332671hg19UCSC Ensembl
Outerchr17:19331351..19332721hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678335
Supporting Variants
SamplesNA18963
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5820083
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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