A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6186569



Internal ID9653450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88237137..88237383hg38UCSC Ensembl
Outerchr16:88237100..88237433hg38UCSC Ensembl
Innerchr16:88270743..88270989hg19UCSC Ensembl
Outerchr16:88270706..88271039hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668088
Supporting Variants
SamplesNA19383
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6186569
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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