A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6153909



Internal ID9885863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151707224..151708832hg38UCSC Ensembl
Outerchr5:151707067..151708985hg38UCSC Ensembl
Innerchr5:151086785..151088393hg19UCSC Ensembl
Outerchr5:151086628..151088546hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664074
Supporting Variants
SamplesNA20761
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6153909
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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