A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15478691



Internal ID4632362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52563979..52575361hg38UCSC Ensembl
Innerchr16:52564224..52575116hg38UCSC Ensembl
Outerchr16:52563734..52575606hg38UCSC Ensembl
chr16:52597891..52609273hg19UCSC Ensembl
Innerchr16:52598136..52609028hg19UCSC Ensembl
Outerchr16:52597646..52609518hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3811383
hg1911383
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638633
Supporting Variants
SamplesHG04162
Known GenesCASC16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15478691
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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