A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5720621



Internal ID8698025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4353329..4362774hg38UCSC Ensembl
Outerchr16:4353172..4362927hg38UCSC Ensembl
Innerchr16:4403330..4412775hg19UCSC Ensembl
Outerchr16:4403173..4412928hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389756
hg199756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659570
Supporting Variants
SamplesNA19058
Known GenesCORO7, CORO7-PAM16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5720621
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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