A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5719071



Internal ID9125280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1357675..1358989hg38UCSC Ensembl
Outerchr16:1357638..1359039hg38UCSC Ensembl
Innerchr16:1407676..1408990hg19UCSC Ensembl
Outerchr16:1407639..1409040hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660383
Supporting Variants
SamplesHG01140
Known GenesGNPTG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5719071
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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