A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638598



Internal ID7025383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49912408..49920683hg38UCSC Ensembl
Innerchr16:49912566..49920525hg38UCSC Ensembl
Outerchr16:49912250..49920841hg38UCSC Ensembl
chr16:49946319..49954594hg19UCSC Ensembl
Innerchr16:49946477..49954436hg19UCSC Ensembl
Outerchr16:49946161..49954752hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg388276
hg198276
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15475560, essv15475562, essv15475561, essv15475563, essv15475559
SamplesNA20321, HG03826, NA12777, NA20867, HG00237
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638598
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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