A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6385314



Internal ID9318089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24529667..24535142hg38UCSC Ensembl
Outerchr16:24529628..24535199hg38UCSC Ensembl
Innerchr16:24540988..24546463hg19UCSC Ensembl
Outerchr16:24540949..24546520hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668750
Supporting Variants
SamplesNA18508
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6385314
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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