A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5964127



Internal ID8941530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3612264..3634219hg38UCSC Ensembl
Outerchr16:3612227..3634269hg38UCSC Ensembl
Innerchr16:3662265..3684220hg19UCSC Ensembl
Outerchr16:3662228..3684270hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822043
hg1922043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668028
Supporting Variants
SamplesHG01389
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5964127
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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